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FDA 510(k) Application Details - K170499
Device Classification Name
More FDA Info for this Device
510(K) Number
K170499
Device Name
sensiLift
Applicant
EL GLOBAL TRADE LTD
8 Tzoran St, P.O. Box 8242
Netanya 4250608 IL
Other 510(k) Applications for this Company
Contact
Yael Liebes-Peer
Other 510(k) Applications for this Contact
Regulation Number
More FDA Info for this Regulation Number
Classification Product Code
PAY
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
02/17/2017
Decision Date
06/15/2017
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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