PROXIDERM (D-460,D 90 460,D 180,460, PS 460)— 510(k) K970439

Name: FDA 510(k) clearance K970439
Creator: U.S. Food and Drug Administration
Published: 1997-04-16

Substantially Equivalent

Progressive Surgical Products, Inc.

FDA 510(k) clearance K970439 for PROXIDERM (D-460,D 90 460,D 180,460, PS 460), Substantially Equivalent on 1997-04-16. 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: 1997-02-05
Decision date: 1997-04-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Westbury, NY, US

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