UNIVERSAL VIDEO/LASER ARM DRAPE— 510(k) K934630

Name: FDA 510(k) clearance K934630
Creator: U.S. Food and Drug Administration
Published: 1994-10-28

Substantially Equivalent

Hydro-Med Products, Inc.

FDA 510(k) clearance K934630 for UNIVERSAL VIDEO/LASER ARM DRAPE, Substantially Equivalent on 1994-10-28. Applicant: Hydro-Med Products, Inc.. Device class: 2.

Clearance details

Applicant: Hydro-Med Products, Inc.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1993-09-24
Decision date: 1994-10-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dallas, TX, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.