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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