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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Cable, Transducer And Electrode, Patient, (Including Connector)
510(k) Number K932704
Device Name PATIENT CABLE
Applicant
Sentry Medical Products, Inc.
17171 Murphy Ave.
Irvine,  CA  92614
Applicant Contact WILLIAM E BLAIR
Correspondent
Sentry Medical Products, Inc.
17171 Murphy Ave.
Irvine,  CA  92614
Correspondent Contact WILLIAM E BLAIR
Regulation Number870.2900
Classification Product Code
DSA  
Date Received06/03/1993
Decision Date 12/27/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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