510(k) K850605 ยท KNW Instrument, Biopsy
RADI-BIOPSY DEVICE
| Applicant | Radiplast AB, Kalamazoo MI, US |
| Decision | Substantially Equivalent, Aug 9, 1985 |
| Received | Feb 15, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850605
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.