510(k) K990064 ยท HQR Apparatus, Cautery, Radiofrequency, Ac-Powered
DI-RHEX OPHTHALMIC DIATHERMY SYSTEM
| Applicant | Ophthalmic Technologies, Inc., Downsview, Ontario, CA |
| Decision | Substantially Equivalent, Apr 4, 1999 |
| Received | Jan 8, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990064
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.