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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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