Gas Sampling Lines 0512
Gas Sampling Lines 0512 is a Class II device made by Salter Labs, LLC, cleared under FDA 510(k) K930957 on 2 Jul 1993 and listed in FDA GUDID since 31 Oct 2023 (UDI-DI 10889483224229), 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 | Number10889483224229 | Date31 Oct 2023 | StatusListed |
| United States | FDA 510(k)SESK | NumberK930957 | Date2 Jul 1993 | StatusActive |
Official records
- AccessGUDID record 10889483224229
- FDA 510(k) database K930957
Across registries
- FDA 510(k) K930957 decided 2 Jul 1993 Active
- FDA GUDID UDI-DI 10889483224229 listed 31 Oct 2023 Listed
Timeline
- Cleared FDA 510(k) K930957
- Listed FDA GUDID 10889483224229
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Gas Sampling Lines
- Generic name
- Nasal oxygen cannula, carbon-dioxide-sampling
- Model / reference
- 0512
- Primary DI / UDI-DI
- 10889483224229
- FDA product code
- CCK
- GMDN term
- Nasal oxygen cannula, carbon-dioxide-sampling
- Device class
- Class II
- Regulation number
- 868.1400
- GUDID distribution status
- In Commercial Distribution