Pacific™ Plus PCP020020180
Pacific™ Plus PCP020020180 is a Class II device made by Medtronic, Inc., cleared under FDA 510(k) K123358 on 29 Jan 2013 and listed in FDA GUDID since 17 Apr 2016 (UDI-DI 08033477044453), 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 | Number08033477044453 | Date17 Apr 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK123358 | Date29 Jan 2013 | StatusActive |
Official records
- AccessGUDID record 08033477044453
- FDA 510(k) database K123358
Across registries
- FDA 510(k) K123358 decided 29 Jan 2013 Active
- FDA GUDID UDI-DI 08033477044453 listed 17 Apr 2016 Listed
Timeline
- Cleared FDA 510(k) K123358
- Listed FDA GUDID 08033477044453
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Pacific™ Plus
- Generic name
- Peripheral angioplasty balloon catheter, basic
- Model / reference
- PCP020020180
- Description
- Cath PCP020020180 Plus US 02L20UL1800
- Primary DI / UDI-DI
- 08033477044453
- 510(k) Number
- FDA product code
- DQY, LIT
- GMDN term
- Peripheral angioplasty balloon catheter, basic
- Device class
- Class II
- Regulation number
- 870.1250
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 20.0 MillimeterOuter Diameter — 2.0 Millimeter
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