IN VITRO T3 RIA TEST — Clinical Assays, Inc. (510(k) K772108)
IN VITRO T3 RIA TEST — Clinical Assays, Inc. (510(k) K772108) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: IN VITRO T3 RIA TEST; Applicant: Clinical Assays, Inc.; Clearance track: 510(k).
| Device name | IN VITRO T3 RIA TEST |
|---|---|
| Applicant | Clinical Assays, Inc. |
| Clearance track | 510(k) |
| Submission number | K772108 |
| Decision | Substantially Equivalent |
| Decision date | 1977-11-17 |
| Date received | 1977-11-07 |
| Product code | CDP |
| Device class | 2 |
| Medical specialty | Clinical Chemistry |
| Applicant location | IL, US |
| Source | openFDA device |
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$1999/mo
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