510(k) K080674 ยท MJG Device, Percutaneous, Biopsy
PAJUNK'S PRIMOCUT DISPOSABLE BIOPSY SYSTEM
| Applicant | PAJUNK GmbH Medizintechnologie, Geisingen, DE |
| Decision | Substantially Equivalent, May 9, 2008 |
| Received | Mar 10, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080674
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.