PROTECTOR RETRACTOR & PROTECTOR RETRACTOR WITH DRAPE— 510(k) K954824

Name: FDA 510(k) clearance K954824
Creator: U.S. Food and Drug Administration
Published: 1996-04-23

Substantially Equivalent

Medical Creative Technologies, Inc.

FDA 510(k) clearance K954824 for PROTECTOR RETRACTOR & PROTECTOR RETRACTOR WITH DRAPE, Substantially Equivalent on 1996-04-23. Applicant: Medical Creative Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Medical Creative Technologies, Inc.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1995-10-20
Decision date: 1996-04-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Colmar, PA, US

Download summary PDF View on FDA.gov ↗

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