FDA 510(k) Applications Submitted by Mike Bunker

FDA 510(k) Number Submission Date Device Name Applicant
K232920 09/19/2023 RELIEFÖ Ureteral Stent Kit; Model: RS-001 - 6 Fr x 24cm, RELIEFÖ Ureteral Stent Kit; Model: RS-002 - 6 Fr x 26cm Ureteral Stent Company
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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