510(k) K060808 ยท HAW Neurological Stereotaxic Instrument
BRAINPRO, BRAINPRO ACCESS
| Applicant | PAJUNK GmbH Medizintechnologie, Geisingen, DE |
| Decision | Substantially Equivalent, Jul 25, 2006 |
| Received | Mar 24, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060808
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.