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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Mattress, Air Flotation, Alternating Pressure
510(k) Number K850419
Device Name AUTO TURNER
Applicant
George J. Kamilar
240 Windsor Ave.
Brightwaters,  NY  11718
Applicant Contact GEORGE J KAMILAR
Correspondent
George J. Kamilar
240 Windsor Ave.
Brightwaters,  NY  11718
Correspondent Contact GEORGE J KAMILAR
Regulation Number880.5550
Classification Product Code
FNM  
Date Received02/04/1985
Decision Date 05/21/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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