PROCEDURE PRODUCTS, INC.

FDA Device Registration & Listing · Vancouver, WA, US · Registration 3020778

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3020778
FEI Number
3020778
Entity Name
PROCEDURE PRODUCTS, INC.
City/State/Country
Vancouver, WA, US
Establishment Address
1801 WEST 4TH PLAIN BLVD., Vancouver, WA 98660, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Procedure Products, Inc. (Owner Number: 3020778)
Owner / Operator Contact Address
1801 WEST 4TH PLAIN BLVD., --, Vancouver, WA 98660, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Polycarbonate and Class VI colors Sterile/Non-sterile 05cc/ml, 10cc/ml and 20cc/ml Plungers for standard BD size barrels and stoppers Syringe, Control and Satndard Color Coded Plungers Along with the polypropylene material 4770 - 1-way stopcock 4¿ tubing and spike Bag Spigots ¿ I.V. Plumbing Adapters ¿ Sterile and Non-sterile 91-722 Univeral Macro Chamber w/ 72¿ line 4722 ¿ Spike with Female luer lock 4771 - 3-way stopcock 4¿ tubing and spike 47-722 Universal Spike w/72¿ line 4721 - Spike with Male Luer Lock 4710 ¿ Bag Spigot with non-vented spike 4709 ¿ Bottle Spigot universal vented spike Polycarbonate - Resin - Polyethylene ! way - 3 way Lock - Slip - Fixed - Configurations Disposable Stopcock - Sterile and Non-sterile Needles, Single Use Catheterization Modified Seldinger Arterial, Chiba, Seldinger without plate, Potts Cournand, SDN 18 ga., 19 ga., 21 ga., Special Procedure Ultra Modified Seldinger, U-KSDN 19 ga. Special , U-SDN 19 ga. Special Legths 1.50 to 9 in., Accepts 15 to 38 wires Ampllatz, BSDN 18 ga., 19 ga., Modified Potts Cournand, KSDN 18 ga., Syringe, Control and Standard Color Coded Plungers 05cc/ml, 10cc/ml and 20cc/ml Plungers for standard BD size barrels and stoppers Polypropylene material and Class VI colors Sterile/Non-sterile Freedom Syringe 4oz cups, 3004-color 2oz cups, 3002-color 8oz cups, 3008-color 16oz cups, 3016-color 32oz cups, 3032-color 4oz cups, 3004-color with lid Color Coded, Blue, Red, Yellow, Green and Semi-clear 2oz cups, 4oz cups with lids, 8oz cups, 16oz cups, sterile and non Polyurethane Lines, Braided Lines, Injector Lines, Pressure Monitoring Lines High Pressure, Standard Pressure Lines Male/Female, Female/Female, Male/Male Configurations Roentgenography Sets and/or Connecting Sets Sizes: OD .110, .140, .155, .187 and .215 Fixed and Rotator ends 1200 PSI, 1000 PSI, 500 PSI and below 10¿, 12¿, 15¿, 20¿ 24¿, 30¿, 36¿, 48¿, 60¿ and 72¿ Lengths 8022 and 8035

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FMF Syringe, Piston General Hospital Class 2 880.5860 2007-12-05
KPE Container, I.V. General Hospital Class 2 880.5025 2007-12-05
FMG Stopcock, I.V. Set General Hospital Class 2 880.5440 2007-12-05
DRE Dilator, Vessel, For Percutaneous Catheterization Cardiovascular Class 2 870.1310 2007-12-05
FMF Syringe, Piston General Hospital Class 2 880.5860 2007-12-05
FMF Syringe, Piston General Hospital Class 2 880.5860 2017-12-22
KYW Container, Liquid Medication, Graduated General Hospital Class 1 880.6430 2012-08-23
DQO Catheter, Intravascular, Diagnostic Cardiovascular Class 2 870.1200 2007-12-05
DQX Wire, Guide, Catheter Cardiovascular Class 2 870.1330 2007-12-05

Official Correspondent

Eric Dietz

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Procedure Products, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K880350 Honway International Co. YUE/FA DISPOSABLE SYRINGE 1988-02-16
K003571 Terumo Medical Corp. SERONO FOR USE WITH GONAL-F 1200IU MULTI-DOSE ONLY AT 600IU/ML SYRINGE 2001-02-12
K041415 B.Braun Medical, Inc. EVA TPN CONTAINER 2004-08-04
K151126 Colibri Technologies, Inc. Foresight Intracardiac Echocardiography (ICE) System 2015-12-18
K931629 Carapace, Inc. CARAPACE ANGIOGRAPHY TRAYS 1993-12-06

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0003-04 Liberty Medical Supplies 2
Liberty brand Insulin Syringes for use with U-100 insulin, 1/2 cc X 30G X 5/16'' syringes
Z-0004-04 Liberty Medical Supplies 2
Liberty brand Insulin Syringes for use with U-100 insulin, 1 cc X 29G X 1/2 '' insulin syringes
Z-0005-04 Liberty Medical Supplies 2
Liberty brand Insulin Syringes for use with U-100 insulin, 1/2 cc X 29G X 1/2 '' insulin syringes
Z-0005-2024 Fresenius Medical Care Holdings, Inc. 2
10ML SYRINGE LUER LOCK W/OUT NEEDLE, Part Number 15-R010-0, 100 per box, 12 boxes to a case
Z-0006-2024 Fresenius Medical Care Holdings, Inc. 2
10ML SYRINGE LUER LOCK W/NEEDLE, Part Number 15-10ML-0, 100 per box, 12 boxes per case

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020778. Last updated year: 2026. Please use registration number 3020778 when referencing this establishment in official correspondence.
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