FDA 510(k) Applications Submitted by Solace Therapeutics, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K170862 03/23/2017 Vesair 0 degree Cystoscope, Vesair 30 degree Long Cystoscope, Vesair 70 degree Long Cystoscope,Vesair 30 degree Cystoscope,Vesair 70 degree Cystoscope Solace Therapeutics, Inc.


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