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FDA 510(k) Applications Submitted by Nitiloop Ltd.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K193322
12/02/2019
NovaCross CTO Microcatheter
Nitiloop Ltd.
K160389
02/11/2016
NovaCross Microcatheter
Nitiloop Ltd.
K172297
07/31/2017
NovaCross Microcatheter
Nitiloop Ltd.
K143608
12/19/2014
NovaCross Microcatheter
Nitiloop Ltd.
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