510(k) K182281 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
Site~Rite 8 Ultrasound System with Cue Needle Tracking System and Pinpoint GT Needle Tech
| Applicant | C. R. Bard, Salt Lake Ciy, UT, US |
| Decision | Substantially Equivalent, Oct 24, 2018 |
| Received | Aug 23, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182281
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.