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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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