510(k) K880659 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
TEKNAR PROSCAN ACCESSORY PROBE
| Applicant | Teknar, Inc., Fenton MO, US |
| Decision | Substantially Equivalent, Apr 14, 1988 |
| Received | Feb 17, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880659
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.