TRIDENT DRAPE SUPPORT— 510(k) K895011

Name: FDA 510(k) clearance K895011
Creator: U.S. Food and Drug Administration
Published: 1989-09-15

Substantially Equivalent

Trident Medical Products, Inc.

FDA 510(k) clearance K895011 for TRIDENT DRAPE SUPPORT, Substantially Equivalent on 1989-09-15. Applicant: Trident Medical Products, Inc.. Device class: 2.

Clearance details

Applicant: Trident Medical Products, Inc.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1989-08-08
Decision date: 1989-09-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Worth, TX, US

Download summary PDF View on FDA.gov ↗

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