K811907 is an FDA 510(k) clearance for the PROGESTERONE DIRECT RIA KIT (125I). This device is classified as a Radioimmunoassay, Progesterone (Class I - General Controls, product code JLS).
Submitted by Immunalysis Corporation (Mchenry, US). The FDA issued a Cleared decision on July 23, 1981, 22 days after receiving the submission on July 1, 1981.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1620.
| 510(k) Number | K811907 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 01, 1981 |
| Decision Date | July 23, 1981 |
| Days to Decision | 22 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | — |
| Product Code | JLS — Radioimmunoassay, Progesterone |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 862.1620 |