MENTOR DBL-COIL INDWELL. SILICONE URETERAL STENT S

Stent, Ureteral

MENTOR CORP.

The following data is part of a premarket notification filed by Mentor Corp. with the FDA for Mentor Dbl-coil Indwell. Silicone Ureteral Stent S.

Pre-market Notification Details

Device IDK850175
510k NumberK850175
Device Name:MENTOR DBL-COIL INDWELL. SILICONE URETERAL STENT S
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 Received1985-01-17
Decision Date1985-03-07

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