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FDA 510(k) Application Details - K181095
Device Classification Name
More FDA Info for this Device
510(K) Number
K181095
Device Name
RF-Relief
Applicant
EL Global Trade Ltd
8 Tzoran St, P.O. Box 8242
Netanya 4250608 IL
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Contact
Martin Gurovich
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Regulation Number
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Classification Product Code
PBX
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Date Received
04/26/2018
Decision Date
07/24/2018
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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