K811459 is an FDA 510(k) clearance for the EMIT-AND METHOTREXATE ASSAY. This device is classified as a Enzyme Immunoassay, Methotrexate.
Submitted by Syva Co. (Mchenry, US). The FDA issued a Cleared decision on June 9, 1981, 14 days after receiving the submission on May 26, 1981.
This device falls under the Chemistry FDA review panel.
| 510(k) Number | K811459 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 26, 1981 |
| Decision Date | June 09, 1981 |
| Days to Decision | 14 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | — |
| Product Code | LAO — Enzyme Immunoassay, Methotrexate |
| Device Class | — |