The following data is part of a premarket notification filed by Amersham Corp. with the FDA for Amerlex Esh Kit.
| Device ID | K820754 |
| 510k Number | K820754 |
| Device Name: | AMERLEX ESH KIT |
| Classification | Radioimmunoassay, Follicle-stimulating Hormone |
| Applicant | AMERSHAM CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CGJ |
| CFR Regulation Number | 862.1300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-03-19 |
| Decision Date | 1982-04-15 |