The following data is part of a premarket notification filed by American Pharmaseal Div. Ahsc with the FDA for Vacu-fil Transfer Set.
| Device ID | K812928 |
| 510k Number | K812928 |
| Device Name: | VACU-FIL TRANSFER SET |
| Classification | Set, I.v. Fluid Transfer |
| Applicant | AMERICAN PHARMASEAL DIV. AHSC 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LHI |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-10-19 |
| Decision Date | 1981-12-30 |