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 ID: K790408
• 510k Number: K790408
• Device Name: T-CONNECTOR
• Classification: Set, Administration, Intravascular
• Applicant: MEDEX, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: FPA
• CFR Regulation Number: 880.5440 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1979-02-26
• Decision Date: 1979-04-30

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
50351688509602	K790408	000
50351688507189	K790408	000
50351688509770	K790408	000
50351688509251	K790408	000
50351688508865	K790408	000
50351688507264	K790408	000
50351688506373	K790408	000
50351688505314	K790408	000
50351688505307	K790408	000
50351688505185	K790408	000
50351688500630	K790408	000
50351688507042	K790408	000
50351688507240	K790408	000
50351688507233	K790408	000
50351688507226	K790408	000
50351688507219	K790408	000
50351688507202	K790408	000
50351688507196	K790408	000
50351688507172	K790408	000
50351688507066	K790408	000
50351688507059	K790408	000
50351688500609	K790408	000