510(k) K931731 ยท HPL Device, Fixation, Ac-Powered, Ophthalmic
STORZ M824 FIXATION DEVICE FOR RETRACTIVE SURGERY
| Applicant | Storz Instrument Co., St. Louis MO, US |
| Decision | Substantially Equivalent, Aug 29, 1994 |
| Received | Apr 7, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931731
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.