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FDA 510(k) Application Details - K971446
Device Classification Name
Electrosurgical, Cutting & Coagulation & Accessories
More FDA Info for this Device
510(K) Number
K971446
Device Name
Electrosurgical, Cutting & Coagulation & Accessories
Applicant
3M COMPANY
3M MEDICAL PRODUCTS GROUP
3M CENTER/275-3E-08
ST. PAUL, MN 55144-1000 US
Other 510(k) Applications for this Company
Contact
LINDA JOHNSEN
Other 510(k) Applications for this Contact
Regulation Number
878.4400
More FDA Info for this Regulation Number
Classification Product Code
GEI
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
04/21/1997
Decision Date
07/18/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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