JOP
- Product code
- JOP
- Device name
- Transducer, Ultrasonic
- Device class
- Class 2
- 21 CFR
- 21 CFR 870.2880
- Medical specialty
- Cardiovascular
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 72
510(k) clearances, last 3 years (2)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K242662 | 2024-12-18 | Viasonix , Ltd. | Falcon/Xpress (Falcon/Xpress) | |
| K233976 | 2024-07-19 | Corvascular Diagnostics, LLC | VasoGuard (V10, V8, V6, V4, V2) |
Official FDA classification page: JOP
Classification and pathway per current FDA publications. Data from openFDA (CC0).