510(k) K161805 ยท KNW Instrument, Biopsy
EnCor MRI Introducer Set, EnCor Probe Introducer
| Applicant | Senorx, Inc., Tempe AZ, US |
| Decision | Substantially Equivalent, Jul 19, 2016 |
| Received | Jul 1, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K161805
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.