GLUCOSE DIAGNOSTIC REAGENT — Connecticut Diagnostics, Ltd. (510(k) K801897)
GLUCOSE DIAGNOSTIC REAGENT — Connecticut Diagnostics, Ltd. (510(k) K801897) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: GLUCOSE DIAGNOSTIC REAGENT; Applicant: Connecticut Diagnostics, Ltd.; Clearance track: 510(k).
| Device name | GLUCOSE DIAGNOSTIC REAGENT |
|---|---|
| Applicant | Connecticut Diagnostics, Ltd. |
| Clearance track | 510(k) |
| Submission number | K801897 |
| Decision | Substantially Equivalent |
| Decision date | 1980-10-10 |
| Date received | 1980-08-08 |
| Product code | CGA |
| Device class | 2 |
| Medical specialty | Clinical Chemistry |
| Applicant location | IL, US |
| Source | openFDA device |
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