510(k) K990238 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
LONGPORT MODEL LDS -1
| Applicant | Longport, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Jun 23, 1999 |
| Received | Jan 25, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990238
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.