510(k) K242852 ยท ETN Stimulator, Nerve
ALM Tube I.D. 6.0, O.D. 8.2 (520843), ALM Tube I.D. 7.0, O.D. 9.7 (520845), ALM Tube I.D. 7.5, O.D. 10.3 (520846), ALM Tube I.D. 8.0, O.D. 11.0 (520847)
| Applicant | Inomed Medizintechnik GmbH, Emmendingen, DE |
| Decision | Substantially Equivalent, Jun 13, 2025 |
| Received | Sep 20, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242852
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.