The following data is part of a premarket notification filed by Becton Dickinson Vascular Access, Inc. with the FDA for Safestart Vascular Access Start Kit.
Device ID | K943941 |
510k Number | K943941 |
Device Name: | SAFESTART VASCULAR ACCESS START KIT |
Classification | I.v. Start Kit |
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 | LRS |
CFR Regulation Number | 880.5200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-08-12 |
Decision Date | 1994-10-20 |