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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Bed, Manual
510(k) Number K881964
Device Name MSI 3003 SERIES BED
Applicant
Med Service, Inc.
P.O. Box 1296
Hwy. 6 W.
Batesville,  MS  38606
Applicant Contact BRUCE BAGGETT
Correspondent
Med Service, Inc.
P.O. Box 1296
Hwy. 6 W.
Batesville,  MS  38606
Correspondent Contact BRUCE BAGGETT
Regulation Number880.5120
Classification Product Code
FNJ  
Date Received05/10/1988
Decision Date 06/28/1988
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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