510(k) K234118
K234118 is an FDA 510(k) premarket notification submitted by ABBOTT MEDICAL for the device "CentriMag Acute Circulatory Support System". The FDA issued a decision of Substantially Equivalent on January 26, 2024. The device falls under product code QNR (Blood Pump For Ecmo, Long-Term (> 6 Hours) Use), a Class II device regulated under 21 CFR 870.4100. ABBOTT MEDICAL has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 26, 2024
- Date Received
- December 28, 2023
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Blood Pump For Ecmo, Long-Term (> 6 Hours) Use
- Device Class
- Class II
- Regulation Number
- 870.4100
- Review Panel
- CV
- Submission Type
A blood pump for long-term circulatory support is a device intended for use as part of an extracorporeal circuit intended to provide assisted extracorporeal circulation and physiologic gas exchange of the patient's blood in patients with acute respiratory failure or acute cardiopulmonary failure where other available treatment options have failed and continued clinical deterioration is expected or the risk of death is imminent.