The following data is part of a premarket notification filed by Vlv Associates, Inc. with the FDA for Vlv Sa Ef Infusion Port.
| Device ID | K953791 |
| 510k Number | K953791 |
| Device Name: | VLV SA EF INFUSION PORT |
| Classification | Set, Administration, Intravascular |
| Applicant | VLV ASSOCIATES, INC. 30-C RIDGEDALE AVE. East Hanover, NJ 07936 |
| Contact | Vincent L Vaillancourt |
| Correspondent | Vincent L Vaillancourt VLV ASSOCIATES, INC. 30-C RIDGEDALE AVE. East Hanover, NJ 07936 |
| Product Code | FPA |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-08-14 |
| Decision Date | 1995-10-30 |