510(k) K933984 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
STORZ FIBEROPTIC REVERSE CUTTING KNIFE
| Applicant | Storz Instrument Co., St. Louis MO, US |
| Decision | Substantially Equivalent, Jan 25, 1994 |
| Received | Aug 16, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933984
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.