Atlas FDA

DLP Aortic Root Cannula, DLP Aortic Root Cannula with Vent Line, DLP Pressure Monitoring Extension Line Adapter, DLP Cardioplegia Adapter with Pressure Port

FDA 510(k) clearance K182586 · decided 2018-10-19

Clearance details

K-number
K182586
Device name
DLP Aortic Root Cannula, DLP Aortic Root Cannula with Vent Line, DLP Pressure Monitoring Extension Line Adapter, DLP Cardioplegia Adapter with Pressure Port
Applicant
Medtronic, Inc.
Decision
Substantially Equivalent
Date received
2018-09-20
Decision date
2018-10-19
Days to decision
29 days
Clearance type
Special
Product code
DWF
Device class
2
Regulation number
870.4210
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Mounds View, MN, US
Third-party review
No
Expedited review
No

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Recalls involving this device

RecordFirmDate
Medtronic Aortic Root Cannulae and Cardioplegia Needles: a) DLP 9 Ga (11 Fr) Aortic Root C recall (Z-1800-2024)Medtronic Perfusion Systems2024-05-10
Medtronic Cardioplegia Adapters: a) DLP 1.8 m (6 ft) Pressure Monitoring Extension Line Ad recall (Z-1801-2024)Medtronic Perfusion Systems2024-05-10

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