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FDA 510(k) Application Details - K131987
Device Classification Name
Powered Laser Surgical Instrument
More FDA Info for this Device
510(K) Number
K131987
Device Name
Powered Laser Surgical Instrument
Applicant
ASCLEPION LASER TECHNOLOGIES GMBH
BRUESSELER STR. 10
JENA, THURINGIA 07747 DE
Other 510(k) Applications for this Company
Contact
ANTJE KATZER
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
06/28/2013
Decision Date
10/15/2014
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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