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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name clip, implantable
510(k) Number K842382
Device Name 3M RAPIDSTAT LIGATING CLIP SYS
Applicant
3M COMPANY
8124 PACIFIC AVE.
WHITE CITY,  OR  97503
Correspondent
3M COMPANY
8124 PACIFIC AVE.
WHITE CITY,  OR  97503
Regulation Number878.4300
Classification Product Code
FZP  
Date Received06/18/1984
Decision Date 08/10/1984
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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