The following data is part of a premarket notification filed by Amersham Corp. with the FDA for Amerlex Lh Ria Kit (code Im2081).
| Device ID | K820753 |
| 510k Number | K820753 |
| Device Name: | AMERLEX LH RIA KIT (CODE IM2081) |
| Classification | Radioimmunoassay, Luteinizing Hormone |
| Applicant | AMERSHAM CORP. 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 | 1982-03-19 |
| Decision Date | 1982-04-09 |