510(k) K031788 ยท MXK Device, Analysis, Anterior Segment
PATHFINDER
| Applicant | Massie Research Laboratories, Inc., Pleasanton CA, US |
| Decision | Substantially Equivalent, Sep 2, 2004 |
| Received | Jun 10, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031788
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.