Maxmixing Block
by Maxtec, Inc.
510(k) K113232
Maxmixing Block is a Class II device made by Maxtec, Inc., cleared under FDA 510(k) K113232 on 1 Mar 2012, 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 | FDA 510(k)SESE | NumberK113232 | Date1 Mar 2012 | StatusActive |
Official records
- FDA 510(k) database K113232
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- BZR
- Device class
- Class II
- Regulation
- 21 CFR Part 868.5330
- Advisory committee
- Anesthesiology
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K113232
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| MaxFlo2 Mini R223P14 | R223P14 | 00817770021827 | On the market | |
| MaxFlo2 R223P01-003 | R223P01-003 | 00853061006050 | No longer on the market | |
| MaxFlo2 R223P01-005 | R223P01-005 | 00853061006135 | No longer on the market | |
| MAXFLO2 R223P01-006 | R223P01-006 | 00817770020783 | No longer on the market | |
| MaxFlo2 R223P02-003 | R223P02-003 | 00853061006067 | No longer on the market | |
| MaxFlo2 R223P02-004 | R223P02-004 | 00853061006036 | No longer on the market | |
| MaxFlo2 R223P02-005 | R223P02-005 | 00853061006142 | No longer on the market | |
| MAXFLO2 R223P02-006 | R223P02-006 | 00817770020790 | No longer on the market | |
| MaxFlo2 R223P02-007 | R223P02-007 | 00853061006159 | No longer on the market | |
| MAXFLO2 R223P08 | R223P08 | 00817770020806 | On the market |
Similar devices
Other devices filed under FDA product code BZR (Mixer, Breathing Gases, Anesthesia Inhalation).
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- LOW FLOW N2O/02O MICROBLENDER by Bird Products Corp.