T3 UPTAKE KIT — E. R. Squibb & Sons, Inc. (510(k) K790417)
T3 UPTAKE KIT — E. R. Squibb & Sons, Inc. (510(k) K790417) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: T3 UPTAKE KIT; Applicant: E. R. Squibb & Sons, Inc.; Clearance track: 510(k).
| Device name | T3 UPTAKE KIT |
|---|---|
| Applicant | E. R. Squibb & Sons, Inc. |
| Clearance track | 510(k) |
| Submission number | K790417 |
| Decision | Substantially Equivalent |
| Decision date | 1979-04-20 |
| Date received | 1979-02-28 |
| Product code | KHQ |
| Device class | 2 |
| Medical specialty | Clinical Chemistry |
| Applicant location | NY, US |
| Source | openFDA device |
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