510(k) K902857 ยท HMY Keratome, Battery-Powered
VISI-DRAPE OPHTHALMIC DRAPES
| Applicant | Visitec Co., Sarasota FL, US |
| Decision | Substantially Equivalent, Jul 31, 1990 |
| Received | Jun 29, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902857
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.