510(k) K212079 ยท KNW Instrument, Biopsy
TeesuVac Breast Biopsy Device Mark 1
| Applicant | Teesuvac Aps, Hoersholm, DK |
| Decision | Substantially Equivalent, Feb 2, 2022 |
| Received | Jul 2, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212079
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.