Dlp® 20009
Dlp 20009 is a cardioplegia cannula (FDA Class II; FDA product code DWF, Catheter, Cannula and Tubing, Vascular, Cardiopulmonary Bypass) made by Medtronic, Inc., cleared under FDA 510(k) K810548 on 17 Mar 1981 and listed in FDA GUDID since 21 May 2016 (UDI-DI 20613994495666), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number20613994495666 | Date21 May 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK810548 | Date17 Mar 1981 | StatusActive |
Official records
- AccessGUDID record 20613994495666
- FDA 510(k) database K810548
Across registries
- FDA 510(k) K810548 decided 17 Mar 1981 Active
- FDA GUDID UDI-DI 20613994495666 listed 21 May 2016 Listed
Timeline
- Cleared FDA 510(k) K810548
- Listed FDA GUDID 20613994495666
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Dlp®
- Generic name
- Cardioplegia cannula
- Model / reference
- 20009
- Primary DI / UDI-DI
- 20613994495666
- 510(k) Number
- FDA product code
- DWF
- GMDN term
- Cardioplegia cannula
- Device class
- Class II
- Regulation number
- 870.4210
- GUDID distribution status
- In Commercial Distribution
- Size
- Catheter Gauge — 11.0 French
Similar devices
Other devices filed under FDA product code DWF (CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS).
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- SARNS TWO-STATE WIRE REINFORCED CATHETER by 3M Health Care, Sarns
- TDMAC-HEPARIN COATED RMI CAROTID BY-PASS SHUNT by Research Medical, Inc.
- AXILLARY ACCESS ARTERIAL CANNULA by Edwards Lifesciences LLC
- TROCAR CATHETER/THORACIC CATHETER by Portex, Ltd.
- CARDIOPULMONARY BYPASS VASCULAR CATHETER by 3M Health Care, Sarns
- MEDTRONIC CLEARVIEW INTRAVASCULAR ARTERIOTOMY SHUNT by MEDTRONIC VASCULAR, INC.