D. O. WEAVER AND COMPANY

FDA Device Registration & Listing · Aurora, CO, US · Registration 1718791

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
1718791
FEI Number
1718791
Entity Name
D. O. WEAVER AND COMPANY
City/State/Country
Aurora, CO, US
Establishment Address
565 NUCLA WAY, UNIT B, Aurora, CO 80011, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
D.O. WEAVER AND COMPANY (Owner Number: 1718791)
Owner / Operator Contact Address
565 NUCLA WAY STE B, --, Aurora, CO 80011, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K883149
PMA Number
N/A

All Registered Proprietary Names

Nuprep Skin Prep Gel Ten20 Conductive Paste

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DRX Electrode, Electrocardiograph Cardiovascular Class 2 870.2360 2007-11-19
GYB Media, Electroconductive Neurology Class 2 882.1275 2007-11-19

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

D.O. WEAVER AND COMPANY
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
K934333 3M Medical Products Group 3M RED DOT 2237 STICKY GEL MONITORING ECG ELECTRODE 1994-07-07

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1718791. Last updated year: 2026. Please use registration number 1718791 when referencing this establishment in official correspondence.
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