Maxventuri R211P38
by Maxtec, Inc.
Maxventuri R211P38 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 9 Nov 2016 (UDI-DI 00817770021148), 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 | GUDID listing | Number00817770021148 | Date9 Nov 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK063488 | Date22 Feb 2007 | StatusActive |
Official records
- AccessGUDID record 00817770021148
- FDA 510(k) database K063488
Across registries
- FDA 510(k) K063488 decided 22 Feb 2007 Active
- FDA GUDID UDI-DI 00817770021148 listed 9 Nov 2016 Listed
Timeline
- Cleared FDA 510(k) K063488
- Listed FDA GUDID 00817770021148
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- Withdrawn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
- R211P38
- Primary DI / UDI-DI
- 00817770021148
- 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
- In Commercial Distribution
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