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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 K863152
Device Name MEDSENTRY FLOTATION SYSTEM
Applicant
Medsentry Corp.
690 El Rancho Rd.
Santa Barbara,  CA  93108
Applicant Contact LAWRENCE BROWNE
Correspondent
Medsentry Corp.
690 El Rancho Rd.
Santa Barbara,  CA  93108
Correspondent Contact LAWRENCE BROWNE
Regulation Number880.5550
Classification Product Code
FNM  
Date Received08/15/1986
Decision Date 09/23/1986
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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