T-CONNECTOR

Set, Administration, Intravascular

MEDEX, INC.

The following data is part of a premarket notification filed by Medex, Inc. with the FDA for T-connector.

Pre-market Notification Details

Device IDK790408
510k NumberK790408
Device Name:T-CONNECTOR
ClassificationSet, Administration, Intravascular
Applicant MEDEX, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeFPA  
CFR Regulation Number880.5440 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1979-02-26
Decision Date1979-04-30

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
50351688509602 K790408 000
50351688507042 K790408 000
50351688507059 K790408 000
50351688507066 K790408 000
50351688507172 K790408 000
50351688507196 K790408 000
50351688507202 K790408 000
50351688507219 K790408 000
50351688507226 K790408 000
50351688507233 K790408 000
50351688507240 K790408 000
50351688500630 K790408 000

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