K014120 is an FDA 510(k) clearance for the TESTOSTERONE BY ENZYMEIMMUNOASSAY (EIA). This device is classified as a Radioimmunoassay, Testosterones And Dihydrotestosterone (Class I - General Controls, product code CDZ).
Submitted by Diagnostics Biochem Canada, Inc. (London, Ontario, CA). The FDA issued a Cleared decision on February 8, 2002, 53 days after receiving the submission on December 17, 2001.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1680.
| 510(k) Number | K014120 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 17, 2001 |
| Decision Date | February 08, 2002 |
| Days to Decision | 53 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
| Product Code | CDZ — Radioimmunoassay, Testosterones And Dihydrotestosterone |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 862.1680 |