DISP. NON-MAGNETIC SURGICAL INSTRU. DRAPE— 510(k) K880513

Name: FDA 510(k) clearance K880513
Creator: U.S. Food and Drug Administration
Published: 1988-03-11

Substantially Equivalent

Taub Industries

FDA 510(k) clearance K880513 for DISP. NON-MAGNETIC SURGICAL INSTRU. DRAPE, Substantially Equivalent on 1988-03-11. Applicant: Taub Industries. Device class: 2.

Clearance details

Applicant: Taub Industries
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1988-02-09
Decision date: 1988-03-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

Download summary PDF View on FDA.gov ↗

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