DERMAHOOK #382-805— 510(k) K771187

Substantially Equivalent

Edward Weck, Inc.

FDA 510(k) clearance K771187 for DERMAHOOK #382-805, Substantially Equivalent on 1977-07-11. Applicant: Edward Weck, Inc.. Device class: 1.

Clearance details

Applicant: Edward Weck, Inc.
Product code: Code GDG
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1977-07-01
Decision date: 1977-07-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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