MaxVenturi R211P39-003
by Maxtec, Inc.
MaxVenturi R211P39-003 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 00817770020905), 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 | Number00817770020905 | Date24 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK063488 | Date22 Feb 2007 | StatusActive |
Official records
- AccessGUDID record 00817770020905
- FDA 510(k) database K063488
Across registries
- FDA 510(k) K063488 decided 22 Feb 2007 Active
- FDA GUDID UDI-DI 00817770020905 listed 24 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K063488
- Listed FDA GUDID 00817770020905
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- Withdrawn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
- R211P39-003
- Primary DI / UDI-DI
- 00817770020905
- 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).
- OXYGEN MONITOR 140/141 by Medix Medical Electronics (U.S.A.), Inc.
- NORMOCAP CR-102, RECORDER UNIT by Instrumentarium-Datex
- MODEL M25R, OXYGEN ANALYZER by Catalyst Research Corp.
- O2-Sensor M-15T incl. Flow diverter 470128 by IT Dr. Gambert GmbH
- O2-Sensor M-04 41 00 06 by IT Dr. Gambert GmbH
- PRO2 Elite Plus Oxygen Analyzer (PRO2PLUS-1) by Salter Labs, LLC
- CARESCAPE B450 MBA313 by GE Healthcare Finland Oy
- OXYMED by Draeger Medical, Inc.
- LC OXYGEN ANALYZER by Ametek/Thermox Instruments Division
- SIEMENS FIO2 SENSOR by SIEMENS MEDICAL SOLUTIONS USA, INC.