510(k) K904845 ยท HNO Keratome, Ac-Powered
STORZ DRAEGER ROTOR KERATOME
| Applicant | Storz Instrument Co., St. Louis MO, US |
| Decision | Substantially Equivalent, Jan 22, 1991 |
| Received | Oct 25, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904845
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.