K890135 is an FDA 510(k) clearance for the IMX FOLLICLE STIMULATING HORMONE (FSH). This device is classified as a Radioimmunoassay, Follicle-stimulating Hormone (Class I - General Controls, product code CGJ).
Submitted by Abbott Laboratories (Abbott Park, US). The FDA issued a Cleared decision on February 10, 1989, 28 days after receiving the submission on January 13, 1989.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1300.
| 510(k) Number | K890135 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 13, 1989 |
| Decision Date | February 10, 1989 |
| Days to Decision | 28 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | — |
| Product Code | CGJ — Radioimmunoassay, Follicle-stimulating Hormone |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 862.1300 |