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FDA 510(k) Application Details - K955006
Device Classification Name
Powered Laser Surgical Instrument
More FDA Info for this Device
510(K) Number
K955006
Device Name
Powered Laser Surgical Instrument
Applicant
CARDIOGENES
P.O. BOX 50875
PALO ALTO, CA 94303 US
Other 510(k) Applications for this Company
Contact
ANNE-MARIE DE MERLIER
Other 510(k) Applications for this Contact
Regulation Number
878.4810
More FDA Info for this Regulation Number
Classification Product Code
GEX
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
11/01/1995
Decision Date
01/17/1996
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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