510(k) K072045 ยท KNW Instrument, Biopsy
ONCONTROL BONE MARROW BIOPSY SYSTEM
| Applicant | Vidacare Corporation, Irvine CA, US |
| Decision | Substantially Equivalent, Oct 22, 2007 |
| Received | Jul 25, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072045
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.