510(k) K262311 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
Alturion Series Diagnostic Ultrasound System
| Applicant | Philips Ultrasound, LLC, Bothell WA, US |
| Decision | Substantially Equivalent, Aug 4, 2026 |
| Received | Jul 8, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K262311
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.