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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 K930626
Device Name SANITAS PATIENT SCALE
Applicant
Dutton-Lainson Co.
451 W. Second St.
Hastings,  NE  68902
Applicant Contact RON HAASE
Correspondent
Dutton-Lainson Co.
451 W. Second St.
Hastings,  NE  68902
Correspondent Contact RON HAASE
Regulation Number880.2720
Classification Product Code
FRW  
Date Received02/08/1993
Decision Date 08/06/1993
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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