ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS311— 510(k) K972086

Name: FDA 510(k) clearance K972086
Creator: U.S. Food and Drug Administration
Published: 1997-08-12

Substantially Equivalent

Alexander Mfg. Co.

FDA 510(k) clearance K972086 for ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS311, Substantially Equivalent on 1997-08-12. Applicant: Alexander Mfg. Co.. Device class: 2.

Clearance details

Applicant: Alexander Mfg. Co.
Product code: Code BZK
Device class: Class 2
Regulation: 21 CFR 868.1850
Advisory panel: Anesthesiology
Date received: 1997-06-04
Decision date: 1997-08-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mason City, IA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code BZK

product code BZK

Death: 2
Total: 2

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.