FDA 510(k) Applications Submitted by Solace Therapeutics

FDA 510(k) Number Submission Date Device Name Applicant
K141252 05/14/2014 GUARDIAN URETHRAL SHEATH SOLACE THERAPEUTICS
K131803 06/19/2013 GUARDIAN URETHRAL SHEATH SOLACE THERAPEUTICS
K162356 08/23/2016 Vesair Cystoscopic Sheath Solace Therapeutics


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