The following data is part of a premarket notification filed by Medex, Inc. with the FDA for T-connector.
| 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 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 50351688509602 | K790408 | 000 |
| 50351688500630 | 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 |
| 50351688507189 | K790408 | 000 |