DISPOS. HYPERBARIC OXYGEN CUSH/TRAUM— 510(k) K831825

Name: FDA 510(k) clearance K831825
Creator: U.S. Food and Drug Administration
Published: 1983-10-27

Substantially Equivalent

Hospitak, Inc.

FDA 510(k) clearance K831825 for DISPOS. HYPERBARIC OXYGEN CUSH/TRAUM, Substantially Equivalent on 1983-10-27. Applicant: Hospitak, Inc.. Device class: 2.

Clearance details

Applicant: Hospitak, Inc.
Product code: Code KPJ
Device class: Class 2
Regulation: 21 CFR 878.5650
Advisory panel: General, Plastic Surgery
Date received: 1983-06-07
Decision date: 1983-10-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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