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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