Ltv 10696
by Vyaire Medical, Inc. 2 variants
Ltv 10696 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 5 Nov 2024 (UDI-DI 10190752201118), 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 | Number10190752201118 | Date5 Nov 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK101643 | Date26 Jan 2011 | StatusActive |
Official records
- AccessGUDID record 10190752201118
- FDA 510(k) database K101643
Across registries
- FDA 510(k) K101643 decided 26 Jan 2011 Active
- FDA GUDID UDI-DI 10190752201118 listed 5 Nov 2024 Listed
Timeline
- Cleared FDA 510(k) K101643
- Listed FDA GUDID 10190752201118
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Ltv
- Generic name
- Ventilator breathing circuit, single-use
- Model / Ref / Catalog
- 10696
- Primary DI / UDI-DI
- 10190752201118
- 510(k) Number
- FDA product code
- CBK
- GMDN term
- Ventilator breathing circuit, single-use
- Device class
- Class II
- Regulation number
- 868.5895
- GUDID distribution status
- In Commercial Distribution
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