BICEPS ELECTROCAUTERY SYSTEM— 510(k) K823755

Name: FDA 510(k) clearance K823755
Creator: U.S. Food and Drug Administration
Published: 1983-01-26

Substantially Equivalent

Squibb Diagnostics

FDA 510(k) clearance K823755 for BICEPS ELECTROCAUTERY SYSTEM, Substantially Equivalent on 1983-01-26. Applicant: Squibb Diagnostics. Device class: 2.

Clearance details

Applicant: Squibb Diagnostics
Product code: Code HAM
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 1982-12-14
Decision date: 1983-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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