OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BED— 510(k) K923710

Name: FDA 510(k) clearance K923710
Creator: U.S. Food and Drug Administration
Published: 1993-03-22

Substantially Equivalent

Progressive Medical Technology, Inc.

FDA 510(k) clearance K923710 for OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BED, Substantially Equivalent on 1993-03-22. Applicant: Progressive Medical Technology, Inc.. Device class: 2.

Clearance details

Applicant: Progressive Medical Technology, Inc.
Product code: Code IKZ
Device class: Class 2
Regulation: 21 CFR 890.5225
Advisory panel: Physical Medicine
Date received: 1992-07-27
Decision date: 1993-03-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lansing, MI, US

Download summary PDF View on FDA.gov ↗

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