510(k) K013396 ยท HAW Neurological Stereotaxic Instrument
ALPHA DRIVE SYSTEM
| Applicant | Alpha Omega , Ltd., Nazareth Illit, IL |
| Decision | Substantially Equivalent, Aug 7, 2002 |
| Received | Oct 15, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K013396
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.