Continuous Ventilator V200-0001-PK
by Flight Medical Innovations Ltd
Continuous Ventilator V200-0001-PK is a Class II device made by Flight Medical Innovations Ltd, cleared under FDA 510(k) K143035 on 30 Mar 2016 and listed in FDA GUDID since 6 Oct 2017 (UDI-DI 17290013641943), 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 | Number17290013641943 | Date6 Oct 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK143035 | Date30 Mar 2016 | StatusActive |
Official records
- AccessGUDID record 17290013641943
- FDA 510(k) database K143035
Across registries
- FDA 510(k) K143035 decided 30 Mar 2016 Active
- FDA GUDID UDI-DI 17290013641943 listed 6 Oct 2017 Listed
Timeline
- Cleared FDA 510(k) K143035
- Listed FDA GUDID 17290013641943
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Continuous Ventilator
- Generic name
- Transport electric ventilator
- Model / reference
- V200-0001-PK
- Primary DI / UDI-DI
- 17290013641943
- 510(k) Number
- FDA product code
- NOU, CBK
- GMDN term
- Transport electric ventilator
- Device class
- Class II
- Regulation number
- 868.5895
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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