Ventlab R500P31
Ventlab R500P31 is a Class II device made by Ventlab Corp., cleared under FDA 510(k) K133540 on 28 Mar 2014 and listed in FDA GUDID since 17 Jul 2023 (UDI-DI 10889483228364), active (FDA 510(k)), not in commercial distribution (GUDID) 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 | Number10889483228364 | Date17 Jul 2023 | StatusListed |
| United States | FDA 510(k)SESE | NumberK133540 | Date28 Mar 2014 | StatusActive |
Official records
- AccessGUDID record 10889483228364
- FDA 510(k) database K133540
Across registries
- FDA 510(k) K133540 decided 28 Mar 2014 Active
- FDA GUDID UDI-DI 10889483228364 listed 17 Jul 2023 Listed
Timeline
- Cleared FDA 510(k) K133540
- Listed FDA GUDID 10889483228364
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Ventlab
- Generic name
- Exhaled-gas oesophageal intubation detector
- Model / Ref / Catalog
- R500P31
- Primary DI / UDI-DI
- 10889483228364
- 510(k) Number
- FDA product code
- CCK
- GMDN term
- Exhaled-gas oesophageal intubation detector
- Device class
- Class II
- Regulation number
- 868.1400
- GUDID distribution status
- Not in Commercial Distribution
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