Power V-Cath 4091-1660
Power V-Cath 4091-1660 is a Class II device made by Neo Medical Inc., cleared under FDA 510(k) K071875 on 5 Nov 2007 and listed in FDA GUDID since 24 Sep 2016 (UDI-DI B339409116600), 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 | NumberB339409116600 | Date24 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK071875 | Date5 Nov 2007 | StatusActive |
Official records
- FDA 510(k) database K071875
Across registries
- FDA 510(k) K071875 decided 5 Nov 2007 Active
- FDA GUDID UDI-DI B339409116600 listed 24 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K071875
- Listed FDA GUDID B339409116600
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Power V-Cath
- Generic name
- Peripherally-inserted central venous catheter
- Model / Ref / Catalog
- 4091-1660
- Primary DI / UDI-DI
- B339409116600
- 510(k) Number
- FDA product code
- LJS
- GMDN term
- Peripherally-inserted central venous catheter
- Device class
- Class II
- Regulation number
- 880.5970
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
- Size
- Pressure — 300 Pound per Square InchLength — 60.0 CentimeterCatheter Gauge — 4.0 French
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