Dlp® 20012
Dlp 20012 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 22 May 2016 (UDI-DI 20613994495505), 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 | Number20613994495505 | Date22 May 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK810548 | Date17 Mar 1981 | StatusActive |
Official records
- AccessGUDID record 20613994495505
- FDA 510(k) database K810548
Across registries
- FDA 510(k) K810548 decided 17 Mar 1981 Active
- FDA GUDID UDI-DI 20613994495505 listed 22 May 2016 Listed
Timeline
- Cleared FDA 510(k) K810548
- Listed FDA GUDID 20613994495505
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Dlp®
- Generic name
- Cardioplegia cannula
- Model / reference
- 20012
- Primary DI / UDI-DI
- 20613994495505
- 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 — 9.0 French
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