Liteaire
510(k) K993101
Liteaire is a Class II device made by Thayer Medical Corporation, cleared under FDA 510(k) K993101 on 26 Oct 2000, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK993101 | Date26 Oct 2000 | StatusActive |
Official records
- FDA 510(k) database K993101
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- CAF
- FDA applicant
- Thayer Medical Corp.
- Device class
- Class II
- Regulation
- 21 CFR Part 868.5630
- Advisory committee
- Anesthesiology
- FDA decision
- SESE Substantially Equivalent