K821380 is an FDA 510(k) clearance for the EMIT TOX ACETAMINOPHEN CONTROL. This device is classified as a Drug Specific Control Materials (Class I - General Controls, product code LAS).
Submitted by Syva Co. (Walker, US). The FDA issued a Cleared decision on June 2, 1982, 23 days after receiving the submission on May 10, 1982.
This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.3280.
| 510(k) Number | K821380 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 10, 1982 |
| Decision Date | June 02, 1982 |
| Days to Decision | 23 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | — |
| Product Code | LAS — Drug Specific Control Materials |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 862.3280 |