The following data is part of a premarket notification filed by Venusa Ltd. with the FDA for Flu Ven I.v. Sets.
| Device ID | K811914 |
| 510k Number | K811914 |
| Device Name: | FLU VEN I.V. SETS |
| Classification | Set, Administration, Intravascular |
| Applicant | VENUSA LTD. 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 | 1981-07-01 |
| Decision Date | 1981-08-03 |