510(k) K212423 · FCG Biopsy Needle
EndoDrill® Model X
| Applicant | Bibbinstruments AB, Lund, SE |
| Decision | Substantially Equivalent, Mar 29, 2023 |
| Received | Aug 4, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212423
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.