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FDA 510(k) Application Details - K955446
Device Classification Name
Cannula, Manipulator/Injector, Uterine
More FDA Info for this Device
510(K) Number
K955446
Device Name
Cannula, Manipulator/Injector, Uterine
Applicant
CONMED CORP.
P.O. BOX 1408
DAYTON, OH 45401-1408 US
Other 510(k) Applications for this Company
Contact
IRA D DUESLER, JR.
Other 510(k) Applications for this Contact
Regulation Number
000.0000
More FDA Info for this Regulation Number
Classification Product Code
LKF
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
11/29/1995
Decision Date
06/18/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OB - Obstetrics/Gynecology
Review Advisory Committee
OB - Obstetrics/Gynecology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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