510(k) K884924 ยท HOF Burr, Corneal, Manual
VISI-WIPE
| Applicant | Visitec Co., Sarasota FL, US |
| Decision | Substantially Equivalent, Jan 31, 1989 |
| Received | Nov 28, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884924
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.