LIGHTCAST II CARBIDE BLADE— 510(k) K760605

Name: FDA 510(k) clearance K760605
Creator: U.S. Food and Drug Administration
Published: 1976-10-05

Substantially Equivalent

Merck, Sharp & Dohme

FDA 510(k) clearance K760605 for LIGHTCAST II CARBIDE BLADE, Substantially Equivalent on 1976-10-05. Applicant: Merck, Sharp & Dohme. Device class: 1.

Clearance details

Applicant: Merck, Sharp & Dohme
Product code: Code GES
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1976-09-08
Decision date: 1976-10-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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