Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015177409

FEI Number

3015177409

Entity Name

DRW MEDICAL

City/State/Country

Aston, PA, US

Establishment Address

2710 Concord Road, Aston, PA 19014, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

DRW Medical, LLC (Owner Number: 10058504)

Owner / Operator Contact Address

2710 Concord Rd., Aston, PA 19014, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K221676

PMA Number

N/A

All Registered Proprietary Names

Exsalta BiDi Catheters Exsalta Disposable Suction Kits FlowPro Nasal Cannulas NAPA Extension Cords NAPA LP-35 Airway Pressure Monitor NAPA LP-15 Power Supply NAPA LP-35 Power Supply NAPA LP-15 Mounting Bracket NAPA LP-15 Airway Pressure Monitor NAPA Pole Clamp NAPA Remote Cables NAPA Sample Line Kits NAPA NP Catheters Exsalta Suction Device

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GAZ	Tubing, Noninvasive	General Hospital	Class 2	880.6740	2026-06-09
BYX	Tubing, Pressure And Accessories	Anesthesiology	Class 1	868.5860	2020-12-14
CAP	Monitor, Airway Pressure (Includes Gauge And/Or Alarm)	Anesthesiology	Class 2	868.2600	2018-10-05
BZO	Set, Tubing And Support, Ventilator (W Harness)	Anesthesiology	Class 1	868.5975	2020-01-15
BTA	Pump, Portable, Aspiration (Manual Or Powered)	General, Plastic Surgery	Class 2	878.4780	2022-12-02

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DRW Medical, LLC

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
K910471	Baxter Healthcare Corp	MEDID-VAC CLEAR NONCONDUCTIVE CONNECTING TUBE	1991-03-08
K812140	3M Company	BIRD MEAN AIRWAY PRESSURE MONITOR	1981-08-20

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0031-2026	Percussionaire Corporation	1	Phasitron 5, IPV In-Line Valve, (Intrapulmonary Percussive Ventilation) REF: P5-TEE-20 (pack of 20)/ P5-TEE (individual) with In-Line Valve Sentec Instructions for Use
Z-0035-2007	Haemonetics Corporation	2	SmartSuction Harmony Powered Suction Device Model Number: HAR-E-115-US

Similar Registrations

Registration Number	Establishment Name	Location
2953726	ADDITION TECHNOLOGY, INC.	Lombard, IL, US
3043534762	AVANTTI MEDI CLEAR MBP, S.A.P.I. DE C.V.	TIJUANA Baja California, MX
3011252788	Changzhou Rongxin Medicine Minimal Invasion Technology Co., Ltd	Jintan Jiangsu, CN
2320762	DEROYAL INDUSTRIES, INC.	NEW TAZEWELL, TN, US
3031231776	Perfect Ophthalmic Instruments FZE	Dubai Dubayy, AE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015177409. Last updated year: 2026. Please use registration number 3015177409 when referencing this establishment in official correspondence.