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FDA 510(k) Applications Submitted by IceCure Medical LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K102360
08/19/2010
ICESENCE 3
ICECURE MEDICAL LTD.
K183213
11/19/2018
IceSense 3, ProSense, MultiSense
IceCure Medical LTD.
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