SYSTEM 2000 REPLACEMENT BATTERY, SYSTEM 2000-EXTENDED RUN REPLACEMENT BATTERY— 510(k) K951450

Name: FDA 510(k) clearance K951450
Creator: U.S. Food and Drug Administration
Published: 1995-05-17

Substantially Equivalent

Strenumed, Inc.

FDA 510(k) clearance K951450 for SYSTEM 2000 REPLACEMENT BATTERY, SYSTEM 2000-EXTENDED RUN REPLACEMENT BATTERY, Substantially Equivalent on 1995-05-17. Applicant: Strenumed, Inc.. Device class: 1.

Clearance details

Applicant: Strenumed, Inc.
Product code: Code KIJ
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1995-03-29
Decision date: 1995-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ventura, CA, US

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