K811809 is an FDA 510(k) clearance for the ANTI-ARRHYTHMIC CONTROL LEVELS I & II. This device is classified as a Drug Mixture Control Materials (Class I - General Controls, product code DIF).
Submitted by Environmental Chemical Specialties (Mchenry, US). The FDA issued a Cleared decision on July 10, 1981, 15 days after receiving the submission on June 25, 1981.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.3280.
| 510(k) Number | K811809 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 25, 1981 |
| Decision Date | July 10, 1981 |
| Days to Decision | 15 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | — |
| Product Code | DIF — Drug Mixture Control Materials |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 862.3280 |