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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 K905061
Device Name APOLLO MOBILE SCALE
Applicant
Apollo Enterprise, Ltd. Co.
P.O. Box 218
Somerset,  WI  54025
Applicant Contact ADRIAN SWEN
Correspondent
Apollo Enterprise, Ltd. Co.
P.O. Box 218
Somerset,  WI  54025
Correspondent Contact ADRIAN SWEN
Regulation Number880.2720
Classification Product Code
FRW  
Date Received11/09/1990
Decision Date 02/12/1991
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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