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FDA 510(k) Application Details - K982984
Device Classification Name
Electrosurgical, Cutting & Coagulation & Accessories
More FDA Info for this Device
510(K) Number
K982984
Device Name
Electrosurgical, Cutting & Coagulation & Accessories
Applicant
MICROLINE PENTAX, INC.
70 WALNUT ST.
WELLESLEY, MA 02481-2102 US
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Contact
JACQUELINE E MASSE
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
08/26/1998
Decision Date
10/21/1998
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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