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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Bed, Flotation Therapy, Powered
510(k) Number K915671
Device Name B.A.S.E. BELLOWS AIR SUPPORT EQUIPMENT
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 Number890.5170
Classification Product Code
IOQ  
Date Received11/25/1991
Decision Date 01/13/1992
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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