BioFlux Device
510(k) K172311
BioFlux Device is a Class II device made by Biotricity, Inc., cleared under FDA 510(k) K172311 on 15 Dec 2017, 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 | NumberK172311 | Date15 Dec 2017 | StatusActive |
Official records
- FDA 510(k) database K172311
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- DXH
- Device class
- Class II
- Regulation
- 21 CFR Part 870.2920
- Advisory committee
- Cardiovascular
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K172311
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 | |||
|---|---|---|---|---|
| BIOFLUX 1.0 | 1.0 | B635BIOFLUX1A0 | — | On the market |
| BIOFLUX 1.0 | 1.0 | B635BIOFLUX100 | — | On the market |
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