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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Instruments, Surgical, Cardiovascular
510(k) Number K882367
Device Name METATECH MICROCLIP APPLICATOR
Applicant
Metatech Corp.
420 Northgate Pkwy.
Wheeling,  IL  60090
Applicant Contact ANTHONY J CIARICO
Correspondent
Metatech Corp.
420 Northgate Pkwy.
Wheeling,  IL  60090
Correspondent Contact ANTHONY J CIARICO
Regulation Number870.4500
Classification Product Code
DWS  
Date Received06/08/1988
Decision Date 08/25/1988
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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