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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 K830171
Device Name DIGITAL BEDSIDE SCALE #5000
Applicant
Acme Medical Scale Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Acme Medical Scale Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number880.2720
Classification Product Code
FRW  
Date Received01/18/1983
Decision Date 02/18/1983
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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