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FDA 510(k) Applications Submitted by Ureteral Stent Company
FDA 510(k) Number
Submission Date
Device Name
Applicant
K213444
10/25/2021
RELIEF Ureteral Stent Kit; Model: RS-001 - 6 Fr x 24cm, RELIEF Ureteral Stent Kit; Model: RS-002 - 6 Fr x 26cm
Ureteral Stent Company
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