510(k) K223596 ยท HAE Rongeur, Manual
SQ.line KERRISON
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Jun 29, 2023 |
| Received | Dec 2, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223596
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.