510(k) K881850 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
TEKNAR PERCU-SCAN
| Applicant | Teknar, Inc., Fenton MO, US |
| Decision | Substantially Equivalent, Aug 29, 1988 |
| Received | May 2, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881850
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.