K854673 is an FDA 510(k) clearance for the DSL ANDROSTENEDIONE RIA (DSL # 4200). This device is classified as a Radioimmunoassay, Androstenedione (Class I - General Controls, product code CIZ).
Submitted by Diagnostic Systems Laboratories, Inc. (Webster, US). The FDA issued a Cleared decision on January 22, 1986, 62 days after receiving the submission on November 21, 1985.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1075.
| 510(k) Number | K854673 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 21, 1985 |
| Decision Date | January 22, 1986 |
| Days to Decision | 62 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | — |
| Product Code | CIZ — Radioimmunoassay, Androstenedione |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 862.1075 |