PROXIDERM (TENTATIVE)— 510(k) K942425

Name: FDA 510(k) clearance K942425
Creator: U.S. Food and Drug Administration
Published: 1994-11-04

Substantially Equivalent

Progressive Surgical Products, Inc.

FDA 510(k) clearance K942425 for PROXIDERM (TENTATIVE), Substantially Equivalent on 1994-11-04. Applicant: Progressive Surgical Products, Inc.. Device class: 1.

Clearance details

Applicant: Progressive Surgical Products, Inc.
Product code: Code MKY
Device class: Class 1
Regulation: 21 CFR 878.4320
Advisory panel: General, Plastic Surgery
Date received: 1994-05-20
Decision date: 1994-11-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Westbury, NY, US

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K962144 — PHOENIX ETE TISSUE EXTENSION SYSTEM1997-01-14
K942526 — SURE-CLOSURE II 75MM SKIN STRETCHING SYSTEM1994-07-19

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