510(k) K021333 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
ARTEMIS
| Applicant | Ultralink, LLC, St Petersburg FL, US |
| Decision | Substantially Equivalent, Oct 8, 2002 |
| Received | Apr 26, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021333
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.