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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Thermometer, Clinical Mercury
510(k) Number K883573
Device Name THERMOMETER, MERCURY/CLINICAL
Applicant
Umax Corp.
Box 683
West Hartford,  CT  06107
Applicant Contact CASS T BYCOSKI
Correspondent
Umax Corp.
Box 683
West Hartford,  CT  06107
Correspondent Contact CASS T BYCOSKI
Regulation Number880.2920
Classification Product Code
FLK  
Date Received08/22/1988
Decision Date 11/07/1988
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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