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FDA 510(k) Applications Submitted by Cathera, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K180959
04/12/2018
Phenom 27 Catheter
Cathera, Inc.
K151638
06/17/2015
Phenom 17 Catheter, Phenom 21 Catheter, Phenom 27 Catheter, Phenom Plus Catheter
Cathera, Inc.
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