ALEXANDER MANUFACTURING RECHARGEABLE BATTERY (M1/T)— 510(k) K970799

Name: FDA 510(k) clearance K970799
Creator: U.S. Food and Drug Administration
Published: 1997-05-14

Substantially Equivalent

Alexander Mfg. Co.

FDA 510(k) clearance K970799 for ALEXANDER MANUFACTURING RECHARGEABLE BATTERY (M1/T), Substantially Equivalent on 1997-05-14. Applicant: Alexander Mfg. Co.. Device class: 2.

Clearance details

Applicant: Alexander Mfg. Co.
Product code: Code LIF
Device class: Class 2
Regulation: 21 CFR 876.5820
Advisory panel: Gastroenterology, Urology
Date received: 1997-03-04
Decision date: 1997-05-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mason City, IA, US

Download summary PDF View on FDA.gov ↗

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