MENTOR UNIVERSAL URETERAL STENT SET

Stent, Ureteral

MENTOR CORP.

The following data is part of a premarket notification filed by Mentor Corp. with the FDA for Mentor Universal Ureteral Stent Set.

Pre-market Notification Details

Device IDK851870
510k NumberK851870
Device Name:MENTOR UNIVERSAL URETERAL STENT SET
ClassificationStent, Ureteral
Applicant MENTOR CORP. 600 PINE AVE. Goleta,  CA  93117
ContactGregory L Johnson
CorrespondentGregory L Johnson
MENTOR CORP. 600 PINE AVE. Goleta,  CA  93117
Product CodeFAD  
CFR Regulation Number876.4620 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1985-04-29
Decision Date1985-07-02

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.