K960412 is an FDA 510(k) clearance for the T-3 MICROWELL EIA MODEL 7013. This device is classified as a Radioimmunoassay, Total Triiodothyronine (Class II - Special Controls, product code CDP).
Submitted by Biomerica, Inc. (Newport Beach, US). The FDA issued a Cleared decision on March 19, 1996, 50 days after receiving the submission on January 29, 1996.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1710.
| 510(k) Number | K960412 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 29, 1996 |
| Decision Date | March 19, 1996 |
| Days to Decision | 50 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
| Product Code | CDP - Radioimmunoassay, Total Triiodothyronine |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.1710 |