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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Clamp, Vascular
510(k) Number K881447
Device Name METATECH METAL MICROCLIP
Applicant
Metatech Corp.
Box 19432
Pittsburgh,  PA  15273
Applicant Contact NIR KOSSOVSKY
Correspondent
Metatech Corp.
Box 19432
Pittsburgh,  PA  15273
Correspondent Contact NIR KOSSOVSKY
Regulation Number870.4450
Classification Product Code
DXC  
Date Received04/06/1988
Decision Date 06/22/1988
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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