SENGEWALD CATALOG NUMBER 55 66 01— 510(k) K863323

Name: FDA 510(k) clearance K863323
Creator: U.S. Food and Drug Administration
Published: 1986-10-29

Substantially Equivalent

Sengewald/USA, Inc.

FDA 510(k) clearance K863323 for SENGEWALD CATALOG NUMBER 55 66 01, Substantially Equivalent on 1986-10-29. Applicant: Sengewald/USA, Inc.. Device class: 2.

Clearance details

Applicant: Sengewald/USA, Inc.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1986-08-27
Decision date: 1986-10-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, US

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