510(k) K030393 ยท MXK Device, Analysis, Anterior Segment
OPTICAL LOW COHERENCE REFLECTOMETRY (OLCR) PACHYMETER
| Applicant | Haag-Streit Holding AG, Rockville MD, US |
| Decision | Substantially Equivalent, Sep 25, 2003 |
| Received | Feb 5, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030393
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.