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FDA 510(k) Application Details - K092761
Device Classification Name
Electrosurgical, Cutting & Coagulation & Accessories
More FDA Info for this Device
510(K) Number
K092761
Device Name
Electrosurgical, Cutting & Coagulation & Accessories
Applicant
BIO PROTECH, INC.
2626 VALLEY VIEW LANE
SUITE 4
DALLAS, TX 75234-6274 US
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Contact
JUDY BURTON
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
09/09/2009
Decision Date
11/24/2009
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Statement
Type
Special
Reviewed By Third Party
N
Expedited Review
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