K883920 is an FDA 510(k) clearance for the EMIT D.A.U. LOW CALIBRATOR A & MEDIUM CALI. A. This device is classified as a Calibrators, Drug Specific (Class II - Special Controls, product code DLJ).
Submitted by Syva Co. (Palo Alto, US). The FDA issued a Cleared decision on October 11, 1988, 25 days after receiving the submission on September 16, 1988.
This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.3200.
| 510(k) Number | K883920 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 16, 1988 |
| Decision Date | October 11, 1988 |
| Days to Decision | 25 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | — |
| Product Code | DLJ — Calibrators, Drug Specific |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.3200 |