510(k) K223300 ยท KNW Instrument, Biopsy
Estacore-Pro Automatic Biopsy Needle, Geotek Semiautomatic Biopsy Needle, Maxicore-M Automatic Biopsy Gun Needle, Maxicore-M Automatic Biopsy Needle and Instrument
| Applicant | Geotek Medikal Ltd Sti, Ankara, TR |
| Decision | Substantially Equivalent, Apr 21, 2023 |
| Received | Oct 27, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223300
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.