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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 K932572
Device Name DIGITAL BABY SCALE MODEL BLB-12
Applicant
Tanita Corp. of America
5200 Church St.
Skokie,  IL  60077
Applicant Contact TOSHIHIKO OSHIMA
Correspondent
Tanita Corp. of America
5200 Church St.
Skokie,  IL  60077
Correspondent Contact TOSHIHIKO OSHIMA
Regulation Number880.2720
Classification Product Code
FRW  
Date Received05/27/1993
Decision Date 11/16/1993
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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