The following data is part of a premarket notification filed by Pcl-ria, Inc. with the FDA for 125-i Labeled Human Luteinizing Hormone.
| Device ID | K780576 |
| 510k Number | K780576 |
| Device Name: | 125-I LABELED HUMAN LUTEINIZING HORMONE |
| Classification | Radioimmunoassay, Luteinizing Hormone |
| Applicant | PCL-RIA, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CEP |
| CFR Regulation Number | 862.1485 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-04-10 |
| Decision Date | 1978-05-19 |