The following data is part of a premarket notification filed by Panmed, Inc. with the FDA for Alfatest.
| Device ID | K780542 |
| 510k Number | K780542 |
| Device Name: | ALFATEST |
| Classification | Ldl & Vldl Precipitation, Hdl |
| Applicant | PANMED, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LBR |
| CFR Regulation Number | 862.1475 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-04-03 |
| Decision Date | 1978-05-19 |