Submission Details
| 510(k) Number | K760078 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | June 18, 1976 |
| Decision Date | July 20, 1976 |
| Days to Decision | 32 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | — |
K760078 is an FDA 510(k) clearance for the REAGENT, RIA TRIIODOTHYRONINE T3 (#200), a Radioimmunoassay, Total Triiodothyronine (Class II — Special Controls, product code CDP), submitted by Oxford Laboratories, Inc. (Mchenry, US). The FDA issued a Cleared decision on July 20, 1976, 32 days after receiving the submission on June 18, 1976. This device falls under the Chemistry review panel. Regulated under 21 CFR 862.1710.
| 510(k) Number | K760078 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | June 18, 1976 |
| Decision Date | July 20, 1976 |
| Days to Decision | 32 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | — |
| Product Code | CDP — Radioimmunoassay, Total Triiodothyronine |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 862.1710 |