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FDA 510(k) Application Details - K161185
Device Classification Name
Powered Laser Surgical Instrument
More FDA Info for this Device
510(K) Number
K161185
Device Name
Powered Laser Surgical Instrument
Applicant
VIAX DENTAL LAB
CALLE POTRERILLOS,
FLEXIPARK BODEGAS D2
ALAJUELA 20108 CR
Other 510(k) Applications for this Company
Contact
EDWIN M. FIRST
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
04/27/2016
Decision Date
09/26/2016
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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