ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500— 510(k) K971826

Name: FDA 510(k) clearance K971826
Creator: U.S. Food and Drug Administration
Published: 1997-07-03

Substantially Equivalent

Alexander Mfg. Co.

FDA 510(k) clearance K971826 for ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500, Substantially Equivalent on 1997-07-03. Applicant: Alexander Mfg. Co.. Device class: 2.

Clearance details

Applicant: Alexander Mfg. Co.
Product code: Code LDR
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 1997-05-16
Decision date: 1997-07-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mason City, IA, US

Download summary PDF View on FDA.gov ↗

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