510(k) K962939 ยท HAW Neurological Stereotaxic Instrument
VECTORVISION
| Applicant | Brainlab, Inc., Moorestown NJ, US |
| Decision | Substantially Equivalent, May 22, 1997 |
| Received | Jul 29, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962939
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.