ABBOTT A-GENT LIQUID MAGNESIUM REAGENT — Abbott Laboratories (510(k) K872311)
ABBOTT A-GENT LIQUID MAGNESIUM REAGENT — Abbott Laboratories (510(k) K872311) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: ABBOTT A-GENT LIQUID MAGNESIUM REAGENT; Applicant: Abbott Laboratories; Clearance track: 510(k).
| Device name | ABBOTT A-GENT LIQUID MAGNESIUM REAGENT |
|---|---|
| Applicant | Abbott Laboratories |
| Clearance track | 510(k) |
| Submission number | K872311 |
| Decision | Substantially Equivalent |
| Decision date | 1987-07-09 |
| Date received | 1987-06-17 |
| Product code | JGJ |
| Device class | 1 |
| Medical specialty | Clinical Chemistry |
| Applicant location | TX, US |
| Source | openFDA device |
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