MICROKNIFE— 510(k) K821769

Name: FDA 510(k) clearance K821769
Creator: U.S. Food and Drug Administration
Published: 1982-09-14

Substantially Equivalent

Biological & Environmental Control Laboratories

FDA 510(k) clearance K821769 for MICROKNIFE, Substantially Equivalent on 1982-09-14. Applicant: Biological & Environmental Control Laboratories. Device class: 1.

Clearance details

Applicant: Biological & Environmental Control Laboratories
Product code: Code EMF
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1982-06-10
Decision date: 1982-09-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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