510(k) K063233 ยท KNW Instrument, Biopsy
DELTACUT (APPARATUS AND CANNULA)
| Applicant | PAJUNK GmbH Medizintechnologie, Geisingen, DE |
| Decision | Substantially Equivalent, Apr 30, 2007 |
| Received | Oct 25, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063233
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.