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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Electrosurgical, Cutting & Coagulation & Accessories
510(k) Number K983871
Device Name RITA MODEL 70 ELECTROSURGICAL PROBE
Applicant
Rita Medical Systems
967 N. Shoreline Blvd.
Mountain View,  CA  94043
Applicant Contact DAVID A TUCKER
Correspondent
Rita Medical Systems
967 N. Shoreline Blvd.
Mountain View,  CA  94043
Correspondent Contact DAVID A TUCKER
Regulation Number878.4400
Classification Product Code
GEI  
Date Received11/02/1998
Decision Date 12/01/1998
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
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