510(k) K072051 ยท DWZ Device, Biopsy, Endomyocardial
NOVATOME, MODEL: SU101-50
| Applicant | Scholten Surgical Instruments, Inc., Lodi CA, US |
| Decision | Substantially Equivalent, Oct 3, 2007 |
| Received | Jul 26, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072051
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.