510(k) K896549 ยท HBI Illuminator, Fiberoptic, Surgical Field
STORZ FIBEROPTIC ENDO-ILLUMINATORS
| Applicant | Storz Instrument Co., St. Louis MO, US |
| Decision | Substantially Equivalent, Feb 15, 1990 |
| Received | Nov 17, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896549
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.