510(k) K061224 ยท HAW Neurological Stereotaxic Instrument
LAPDOC I
| Applicant | Robodent GmbH, Berlin, DE |
| Decision | Substantially Equivalent, Sep 5, 2006 |
| Received | May 1, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061224
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.