The following data is part of a premarket notification filed by General Diagnostics with the FDA for H-d-el.
| Device ID | K790372 |
| 510k Number | K790372 |
| Device Name: | H-D-EL |
| Classification | Ldl & Vldl Precipitation, Hdl |
| Applicant | GENERAL DIAGNOSTICS 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 | 1979-02-23 |
| Decision Date | 1979-05-03 |