QUALI-MED'S OPERATING ROOM DRAPES— 510(k) K862172

Name: FDA 510(k) clearance K862172
Creator: U.S. Food and Drug Administration
Published: 1986-06-19

Substantially Equivalent

Quali-Med, Inc.

FDA 510(k) clearance K862172 for QUALI-MED'S OPERATING ROOM DRAPES, Substantially Equivalent on 1986-06-19. Applicant: Quali-Med, Inc.. Device class: 2.

Clearance details

Applicant: Quali-Med, Inc.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1986-06-09
Decision date: 1986-06-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sugar Land, TX, US

Download summary PDF View on FDA.gov ↗

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