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FDA 510(k) Application Details - K981919
Device Classification Name
Electrosurgical, Cutting & Coagulation & Accessories
More FDA Info for this Device
510(K) Number
K981919
Device Name
Electrosurgical, Cutting & Coagulation & Accessories
Applicant
GUENTER BISSINGER MEDIZINTECHNIK GMBH
GOTTLIEB-DAIMLER-STR. 5
(ROHRLACHE)
TENINGEN D-79331 DE
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Contact
DAGMAR S MASER
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
06/01/1998
Decision Date
08/06/1998
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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