MODIFICATION TO SYNCHRON LX CLINICAL CHEMISTRY SYSTEMS (LX20 AND LX20 PRO)
FDA 510(k) clearance K014034 · decided 2001-12-18
Clearance details
- K-number
- K014034
- Device name
- MODIFICATION TO SYNCHRON LX CLINICAL CHEMISTRY SYSTEMS (LX20 AND LX20 PRO)
- Applicant
- Beckman Coulter, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2001-12-07
- Decision date
- 2001-12-18
- Days to decision
- 11 days
- Clearance type
- Special
- Product code
- JFL
- Device class
- 2
- Regulation number
- 862.1160
- Medical specialty
- Clinical Chemistry
- Advisory committee
- Clinical Chemistry
- Location
- Brea, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| Synchron LX Clinical Systems, Operating Software, All versions. recall (Z-1098-04) | Beckman Coulter Inc | 2004-07-20 |
| Synchron LX Clinical Systems Software recall (Z-1116-04) | Beckman Coulter Inc | 2004-07-20 |
| Synchron CX Systems version 4.0 Operating Software used in Synchron LX20 Systems, Synchron recall (Z-0096-04) | Beckman Coulter Inc | 2003-11-06 |
| SYNCHRON LX20 AND LX20 Pro recall (Z-0545-03) | Beckman Coulter Inc | 2003-02-05 |
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| Access AFP (on DxI 9000 Analyzer) (P980041/S051) | Beckman Coulter, Inc. | 2025-11-03 |
| Access HBsAg, Access HBsAg Confirmatory, Access HBsAg Calibrator, Access HBsAg QC (P230015) | Beckman Coulter, Inc. | 2025-10-17 |
| Access Hybritech p2PSA (P090026/S032) | Beckman Coulter, Inc. | 2025-06-16 |
| Access Hybritech free PSA (P970038/S046) | Beckman Coulter, Inc. | 2025-05-15 |
| Access Hybritech PSA (P850048/S060) | Beckman Coulter, Inc. | 2024-09-04 |
| Access Hybritech PSA reagent pack (P850048/S059) | Beckman Coulter, Inc. | 2023-05-25 |
| Access AFP Reagents on the Access Immunoassay Systems (P980041/S050) | Beckman Coulter, Inc. | 2022-12-16 |
| Access Hybritech PSA Reagents on the Access Immunoassay Systems (P850048/S057) | Beckman Coulter, Inc. | 2022-12-16 |