MODIFICATION TO ZAP GUARD DEFIBRILLATOR TEST PROBE— 510(k) K030547

Name: FDA 510(k) clearance K030547
Creator: U.S. Food and Drug Administration
Published: 2003-07-11

Substantially Equivalent

Guardian Angel Products, Inc.

FDA 510(k) clearance K030547 for MODIFICATION TO ZAP GUARD DEFIBRILLATOR TEST PROBE, Substantially Equivalent on 2003-07-11. Applicant: Guardian Angel Products, Inc.. Device class: 2.

Clearance details

Applicant: Guardian Angel Products, Inc.
Product code: Code DRL
Device class: Class 2
Regulation: 21 CFR 870.5325
Advisory panel: Cardiovascular
Date received: 2003-02-20
Decision date: 2003-07-11
Decision: Substantially Equivalent
Clearance type: Special
Location: Huntingdon Valley, PA, US

Download summary PDF View on FDA.gov ↗

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