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FDA 510(k) Application Details - K102913
Device Classification Name
Electrosurgical, Cutting & Coagulation & Accessories
More FDA Info for this Device
510(K) Number
K102913
Device Name
Electrosurgical, Cutting & Coagulation & Accessories
Applicant
COVIDIEN, FORMERLY VALLEYLAB, A DIVISION OF TYCO H
5920 LONGBOW DRIVE
BOULDER, CO 80301 US
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Contact
BEN CORDILEONE
Other 510(k) Applications for this Contact
Regulation Number
878.4400
More FDA Info for this Regulation Number
Classification Product Code
GEI
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More FDA Info for this Product Code
Date Received
10/01/2010
Decision Date
05/06/2011
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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