510(k) K924999 ยท KYG Device, Irrigation, Ocular Surgery
AUTOPOLE REGULATOR SYSTEM
| Applicant | Escalon Trek Medical, Skillmanl NJ, US |
| Decision | Substantially Equivalent, Dec 24, 1992 |
| Received | Oct 2, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924999
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.