510(k) K183235 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
SonoSite SII Ultrasound System
| Applicant | FUJIFILM Sonosite, Inc., Bothell WA, US |
| Decision | Substantially Equivalent, Feb 7, 2019 |
| Received | Nov 20, 2018 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K183235
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.