IMPULSE 3000 DEFIBRILLATOR ANALYZER— 510(k) K934254

Name: FDA 510(k) clearance K934254
Creator: U.S. Food and Drug Administration
Published: 1993-11-23

Substantially Equivalent

Dynatech/Nevada, Inc.

FDA 510(k) clearance K934254 for IMPULSE 3000 DEFIBRILLATOR ANALYZER, Substantially Equivalent on 1993-11-23. Applicant: Dynatech/Nevada, Inc.. Device class: 2.

Clearance details

Applicant: Dynatech/Nevada, Inc.
Product code: Code DRL
Device class: Class 2
Regulation: 21 CFR 870.5325
Advisory panel: Cardiovascular
Date received: 1993-08-31
Decision date: 1993-11-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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