K811461 is an FDA 510(k) clearance for the EMIT-AND METHOTREXATE CONTROL. This device is classified as a N-acetylprocainamide Control Materials (Class I - General Controls, product code LAZ).
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 Toxicology FDA review panel. Regulated under 21 CFR 862.3280.
| 510(k) Number | K811461 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 | Toxicology (TX) |
| Summary | — |
| Product Code | LAZ — N-acetylprocainamide Control Materials |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 862.3280 |