IMPULSE 3000 DEFIBRILLATOR ANALYZER— 510(k) K934254

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..

Clearance details

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

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