Company ยท US
Biotricity
FDA 510(k) clearances and medical device recalls filed under this name, 2016 to 2022. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|
| DSH | Recorder, Magnetic Tape, Medical | 2 |
| MWJ | Electrocardiograph, Ambulatory (Without Analysis) | 2 |
| DXH | Transmitters And Receivers, Electrocardiograph, Telephone | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|
| Jul 28, 2022 | K222017 | Biotres Biotricity | MWJ |
| Jan 19, 2022 | K211709 | Biotres Biotricity | MWJ |
| Jul 29, 2020 | K201040 | Bioflux Software II Biotricity | DSH |
| Dec 15, 2017 | K172311 | BioFlux Device Biotricity, Inc. | DXH |
| Oct 13, 2016 | K162571 | Bioflux Software Biotricity, Inc., CA | DSH |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|
| No recalls in this window. |