Ltv 14982-001
Ltv 14982-001 is a Class II device made by Vyaire Medical, Inc., cleared under FDA 510(k) K101643 on 26 Jan 2011 and listed in FDA GUDID since 19 Mar 2021 (UDI-DI 10190752129320), 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 | Number10190752129320 | Date19 Mar 2021 | StatusListed |
| United States | FDA 510(k)SESE | NumberK101643 | Date26 Jan 2011 | StatusActive |
Official records
- AccessGUDID record 10190752129320
- FDA 510(k) database K101643
Across registries
- FDA 510(k) K101643 decided 26 Jan 2011 Active
- FDA GUDID UDI-DI 10190752129320 listed 19 Mar 2021 Listed
Timeline
- Cleared FDA 510(k) K101643
- Listed FDA GUDID 10190752129320
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Ltv
- Generic name
- Ventilator stand
- Model / Ref / Catalog
- 14982-001
- Primary DI / UDI-DI
- 10190752129320
- 510(k) Number
- FDA product code
- CBK
- GMDN term
- Ventilator stand
- Device class
- Class II
- Regulation number
- 868.5895
- GUDID distribution status
- In Commercial Distribution
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