510(k) K051940 ยท MXK Device, Analysis, Anterior Segment
CM 3910 ROTATING DOUBLE SCHEIMPFLUG CAMERA
| Applicant | Sis Ltd., Surgical Instrument Systems, Littleton CO, US |
| Decision | Substantially Equivalent, Sep 28, 2005 |
| Received | Jul 18, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K051940
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.