510(k) K897034 ยท HOZ Sponge, Ophthalmic
K-SPONGE
| Applicant | Katena Products, Inc., Denville NJ, US |
| Decision | Substantially Equivalent, Feb 15, 1990 |
| Received | Dec 18, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K897034
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.