510(k) K231422 ยท FCG Biopsy Needle
Precision GI
| Applicant | Limaca Medical, Ltd., En Ha'Emeq, IL |
| Decision | Substantially Equivalent, Aug 28, 2023 |
| Received | May 17, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231422
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.