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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Bed, Patient Rotation, Powered
510(k) Number K923710
Device Name OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BED
Applicant
Progressive Medical Technology, Inc.
815 Terminal Rd.
Lansing,  MI  48906
Applicant Contact VAN DYKE
Correspondent
Progressive Medical Technology, Inc.
815 Terminal Rd.
Lansing,  MI  48906
Correspondent Contact VAN DYKE
Regulation Number890.5225
Classification Product Code
IKZ  
Date Received07/27/1992
Decision Date 03/22/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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