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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name instrument, surgical, disposable
510(k) Number K810080
Device Name VASCULAR TIE (VAS-TIE)
Applicant
SIL-MED CORP.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
SIL-MED CORP.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number878.4800
Classification Product Code
KDC  
Date Received01/13/1981
Decision Date 04/02/1981
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
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