510(k) K000728 ยท FST Light, Surgical, Fiberoptic
MEDTRONIC SOLAN FIBEROPTIC CORNEAL LIGHT PROBE
| Applicant | Medtronic Xomed, Jacksonville FL, US |
| Decision | Substantially Equivalent, Mar 21, 2000 |
| Received | Mar 6, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000728
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.