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FDA 510(k) Applications Submitted by 3NT Medical Ltd.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K181838
07/10/2018
Sinusway Dilation System
3NT Medical Ltd.
K192305
08/23/2019
Colibri Endoscopy System
3NT Medical Ltd.
K202727
09/17/2020
Peregrine Endoscopy System
3NT Medical Ltd.
K162916
10/17/2016
3NT endoscopy system
3NT Medical Ltd.
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