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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 K822135
Device Name SECA DIGITAL BABY SCALE 727
Applicant
Seca Corp.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Seca Corp.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number880.2720
Classification Product Code
FRW  
Date Received07/20/1982
Decision Date 07/30/1982
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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