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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Scale, Patient
510(k) Number K910583
Device Name U.S. MEDICAL PS-3000 NEONATAL SCALE
Applicant
U.S. Medical Corp.
408 Highland Avenlue
P.O. Box 580
Cheshire,  CT  06410
Applicant Contact BRUCE E DODSON
Correspondent
U.S. Medical Corp.
408 Highland Avenlue
P.O. Box 580
Cheshire,  CT  06410
Correspondent Contact BRUCE E DODSON
Regulation Number880.2720
Classification Product Code
FRW  
Date Received02/11/1991
Decision Date 03/21/1991
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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