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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K832272
Device Name TOURNIQUET CUFF PRESSURE MONITOR #TCPM
Applicant
Electromedics, Inc.
IN 
Correspondent
Electromedics, Inc.
IN 
Classification Product Code
LDQ
Date Received07/12/1983
Decision Date 11/28/1983
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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