Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2921581

FEI Number

2921581

Entity Name

FLUKE BIOMEDICAL

City/State/Country

EVERETT, WA, US

Establishment Address

6920 SEAWAY BLVD., EVERETT, WA 98203, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

FLUKE ELECTRONICS CORP. (Owner Number: 9031860)

Owner / Operator Contact Address

6920 SEAWAY BLVD., --, Everett, WA 98203, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Impulse 7010 Clear-Pb

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DRL	Tester, Defibrillator	Cardiovascular	Class 2	870.5325	2010-07-27
KPY	Shield, Protective, Personnel	Radiology	Class 1	892.6500	2006-01-25

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

FLUKE ELECTRONICS CORP.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2921581. Last updated year: 2026. Please use registration number 2921581 when referencing this establishment in official correspondence.