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FDA 510(k) Application Details - K122278
Device Classification Name
Electrosurgical, Cutting & Coagulation & Accessories
More FDA Info for this Device
510(K) Number
K122278
Device Name
Electrosurgical, Cutting & Coagulation & Accessories
Applicant
BAYLIS MEDICAL COMPANY INC.
2645 MATHESON BLVD. EAST
MISSISSAUGA L4W 5S4 CA
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Contact
MEGHAL KHAKHAR
Other 510(k) Applications for this Contact
Regulation Number
878.4400
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Classification Product Code
GEI
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More FDA Info for this Product Code
Date Received
07/30/2012
Decision Date
11/07/2012
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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