SYNCHRON LX I 725 CLINICAL SYSTEM — Beckman Coulter, Inc. (510(k) K023049)
SYNCHRON LX I 725 CLINICAL SYSTEM — Beckman Coulter, Inc. (510(k) K023049) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: SYNCHRON LX I 725 CLINICAL SYSTEM; Applicant: Beckman Coulter, Inc.; Clearance track: 510(k).
| Device name | SYNCHRON LX I 725 CLINICAL SYSTEM |
|---|---|
| Applicant | Beckman Coulter, Inc. |
| Clearance track | 510(k) |
| Submission number | K023049 |
| Decision | Substantially Equivalent |
| Decision date | 2002-10-04 |
| Date received | 2002-09-12 |
| Product code | JGS |
| Device class | 2 |
| Medical specialty | Clinical Chemistry |
| Applicant location | CA, US |
| Source | openFDA device |
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