The following data is part of a premarket notification filed by Becton Dickinson Vascular Access, Inc. with the FDA for E-z Set(r) And Minicath(r) Infusion Sets.
| Device ID | K950302 |
| 510k Number | K950302 |
| Device Name: | E-Z SET(R) AND MINICATH(R) INFUSION SETS |
| Classification | Set, Administration, Intravascular |
| Applicant | BECTON DICKINSON VASCULAR ACCESS, INC. 9450 SOUTH STATE ST. Sandy, UT 84070 |
| Contact | C J Welle |
| Correspondent | C J Welle BECTON DICKINSON VASCULAR ACCESS, INC. 9450 SOUTH STATE ST. Sandy, UT 84070 |
| Product Code | FPA |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-01-25 |
| Decision Date | 1995-03-13 |