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Percuflex Ureteral Stent System, Percuflex Ureteral Stent System Kit, Percuflex Nephroureteral Stent System, Amplatz Anchor Catheter System

Boston Scientific Corporation · Class II · Cleared Apr 26, 2021

K-numberK200260
Device namePercuflex Ureteral Stent System, Percuflex Ureteral Stent System Kit, Percuflex Nephroureteral Stent System, Amplatz Anchor Catheter System
ApplicantBoston Scientific Corporation
Product codeFAD
Device classClass II
Decision dateApr 26, 2021
DecisionUnknown
Regulation876.4620
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View the full FDA submission: accessdata.fda.gov

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