DIGOXIN-EIA-XT — In Vitro Diagnostics, Inc. (510(k) K896863)
DIGOXIN-EIA-XT — In Vitro Diagnostics, Inc. (510(k) K896863) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: DIGOXIN-EIA-XT; Applicant: In Vitro Diagnostics, Inc.; Clearance track: 510(k).
| Device name | DIGOXIN-EIA-XT |
|---|---|
| Applicant | In Vitro Diagnostics, Inc. |
| Clearance track | 510(k) |
| Submission number | K896863 |
| Decision | Substantially Equivalent |
| Decision date | 1990-02-13 |
| Date received | 1989-12-06 |
| Product code | KXT |
| Device class | 2 |
| Medical specialty | Clinical Toxicology |
| Applicant location | CO, US |
| Source | openFDA device |
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$1999/mo
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