510(k) K042742 ยท MXK Device, Analysis, Anterior Segment
HEIDELBERG RETINA TOMOGRAPH II / ROSTOCK CORNEA MODULE (HRT II / RCM)
| Applicant | Heidelberg Engineering, Dossenheim, DE |
| Decision | Substantially Equivalent, Oct 13, 2004 |
| Received | Oct 4, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042742
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.