510(k) K882162 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
NIDEK US-3000
| Applicant | Nidek, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Aug 19, 1988 |
| Received | May 23, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882162
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.