PROXIDERM, MODELS TN 460, TN 90 460, BK 460— 510(k) K982439

Name: FDA 510(k) clearance K982439
Creator: U.S. Food and Drug Administration
Published: 1998-09-08

Substantially Equivalent

Progressive Surgical Products, Inc.

FDA 510(k) clearance K982439 for PROXIDERM, MODELS TN 460, TN 90 460, BK 460, Substantially Equivalent on 1998-09-08. 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: 1998-07-14
Decision date: 1998-09-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Westbury, NY, US

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