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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 K942321
Device Name VARIOUSPATIENT MONITORING CABLE
Applicant
Merit Cables Incorporated
3199 Airport Loop Dr.
Costa Mesa,  CA  92626
Applicant Contact RONALD L BALLARD
Correspondent
Merit Cables Incorporated
3199 Airport Loop Dr.
Costa Mesa,  CA  92626
Correspondent Contact RONALD L BALLARD
Regulation Number870.2900
Classification Product Code
DSA  
Date Received05/13/1994
Decision Date 11/04/1994
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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