510(k) K251103 ยท OBJ Catheter, Ultrasound, Intravascular
VeriSight Intracardiac Echocardiography Catheter (VSICE2D); VeriSight Pro Intracardiac Echocardiography Catheter (VSICE3D)
| Applicant | Philips Image Guided Therapy Corporation, San Diego CA, US |
| Decision | Substantially Equivalent, May 9, 2025 |
| Received | Apr 11, 2025 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K251103
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.