MIDMARK MIDLINE CATHETER

Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days

MENLO CARE, INC.

The following data is part of a premarket notification filed by Menlo Care, Inc. with the FDA for Midmark Midline Catheter.

Pre-market Notification Details

Device IDK951620
510k NumberK951620
Device Name:MIDMARK MIDLINE CATHETER
ClassificationCatheter, Intravascular, Therapeutic, Short-term Less Than 30 Days
Applicant MENLO CARE, INC. 1350 WILLOW RD. Menlo Park,  CA  94025 -1516
ContactThomas Lawson
CorrespondentThomas Lawson
MENLO CARE, INC. 1350 WILLOW RD. Menlo Park,  CA  94025 -1516
Product CodeFOZ  
CFR Regulation Number880.5200 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1995-04-07
Decision Date1996-04-04
Summary:summary

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