CentriMag Pre-connected Pack
FDA 510(k) clearance K222297 · decided 2022-12-01
Clearance details
- K-number
- K222297
- Device name
- CentriMag Pre-connected Pack
- Applicant
- Abbott
- Decision
- Substantially Equivalent
- Date received
- 2022-08-01
- Decision date
- 2022-12-01
- Days to decision
- 122 days
- Clearance type
- Traditional
- Product code
- DTZ
- Device class
- 2
- Regulation number
- 870.4350
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Pleasanton, CA, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| CentriMag Circulatory Support System (P170038/S025) | Abbott | 2025-12-01 |
| CentriMag Circulatory Support System (P170038/S023) | Abbott | 2025-09-29 |
| CentriMag Circulatory Support System (P170038/S026) | Abbott | 2025-08-21 |
| CentriMag Circulatory Support System (P170038/S024) | Abbott | 2025-06-02 |
| CentriMag Circulatory Support System (P170038/S017) | Abbott | 2025-02-04 |
| CentriMag Circulatory Support System (P170038/S022) | Abbott | 2024-11-05 |
| CentriMag Circulatory Support System (P170038/S021) | Abbott | 2024-11-01 |
| CentriMag Circulatory Support System (P170038/S020) | Abbott | 2024-09-25 |