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FDA 510(k) Application Details - K072779
Device Classification Name
Powered Laser Surgical Instrument
More FDA Info for this Device
510(K) Number
K072779
Device Name
Powered Laser Surgical Instrument
Applicant
BIOLITEC, INC.
555 THIRTEENTH ST., NW
WASHINGTON, DC 20004-5910 US
Other 510(k) Applications for this Company
Contact
JONATHAN S KAHAN
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
09/28/2007
Decision Date
01/24/2008
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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