MaxVenturi R211P39-002
by Maxtec, Inc.
MaxVenturi R211P39-002 is a Class II device made by Maxtec, Inc., cleared under FDA 510(k) K063488 on 22 Feb 2007 and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00817770020899), active (FDA 510(k)), not in commercial distribution (GUDID) 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 | GUDID listing | Number00817770020899 | Date24 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK063488 | Date22 Feb 2007 | StatusActive |
Official records
- AccessGUDID record 00817770020899
- FDA 510(k) database K063488
Across registries
- FDA 510(k) K063488 decided 22 Feb 2007 Active
- FDA GUDID UDI-DI 00817770020899 listed 24 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K063488
- Listed FDA GUDID 00817770020899
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- MaxVenturi
- Generic name
- Respiratory oxygen monitor, battery-powered
- Model / reference
- R211P39-002
- Primary DI / UDI-DI
- 00817770020899
- 510(k) Number
- FDA product code
- CCL
- GMDN term
- Respiratory oxygen monitor, battery-powered
- Device class
- Class II
- Regulation number
- 868.1720
- GUDID distribution status
- Not in Commercial Distribution
Similar devices
Other devices filed under FDA product code CCL (Analyzer, Gas, Oxygen, Gaseous-Phase).
- O2-Sensor M-25 incl. Flow Diverter 410420 by IT Dr. Gambert GmbH
- O2-Sensor M-15TL incl. Flow diverter 410423 by IT Dr. Gambert GmbH
- OHMEDA 5120 OXYGEN MONITOR by Ohmeda Medical
- OPTION A02 MODEL 15202A by Hewlett-Packard Co.
- MODEL A-1 OXYGEN ANALYZER by Medical, Inc.
- OXYGEN ANALYZER 200 by SALTER LABS
- BIOCHEM TEMPERATURE/ FIO2 MODULE by Biochem International, Inc.
- O2 TEST by Erich Jaeger GmbH
- SL02 OXYGEN ANALYZER by SALTER LABS
- CARESCAPE Canvas Smart Display 5897060 by GE Healthcare Finland Oy