K832493 is an FDA 510(k) clearance for the QUINIDINE FLUORESCENT IMMUNOASSAY. This device is classified as a Enzyme Immunoassay, Quinidine (Class II - Special Controls, product code LBZ).
Submitted by American Diagnostic Corp. (Mchenry, US). The FDA issued a Cleared decision on September 12, 1983, 47 days after receiving the submission on July 27, 1983.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.3320.
| 510(k) Number | K832493 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 27, 1983 |
| Decision Date | September 12, 1983 |
| Days to Decision | 47 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | — |
| Product Code | LBZ — Enzyme Immunoassay, Quinidine |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.3320 |