MENTOR PERCUTANEOUS COIL NEPHROSTOMY SET

Catheter, Nephrostomy

MENTOR CORP.

The following data is part of a premarket notification filed by Mentor Corp. with the FDA for Mentor Percutaneous Coil Nephrostomy Set.

Pre-market Notification Details

Device IDK850286
510k NumberK850286
Device Name:MENTOR PERCUTANEOUS COIL NEPHROSTOMY SET
ClassificationCatheter, Nephrostomy
Applicant MENTOR CORP. 600 PINE AVE. Goleta,  CA  93117
ContactGregory L Johnson
CorrespondentGregory L Johnson
MENTOR CORP. 600 PINE AVE. Goleta,  CA  93117
Product CodeLJE  
CFR Regulation Number510(k) Premarket Notification [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1985-01-24
Decision Date1985-02-28

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