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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 K862477
Device Name HOYER DIGITAL ELECTRONIC SCALE
Applicant
Ted Hoyer & Co., Inc.
2222 Minnesota St.
P.O. Box 2744
Oshkosh,  WI  54903
Applicant Contact S. C SCHUPPE
Correspondent
Ted Hoyer & Co., Inc.
2222 Minnesota St.
P.O. Box 2744
Oshkosh,  WI  54903
Correspondent Contact S. C SCHUPPE
Regulation Number880.2720
Classification Product Code
FRW  
Date Received06/30/1986
Decision Date 09/03/1986
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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