510(k) K240706 ยท JEH Plethysmograph, Volume
PowerCube+ Series (PowerCube Body+); PowerCube+ Series (PowerCube Diffusion+); PowerCube+ Series (PowerCube Body+ / Diffusion+)
| Applicant | Ganshorn Medizin Electronic GmbH, Niederlauer, DE |
| Decision | Substantially Equivalent, Dec 9, 2024 |
| Received | Mar 14, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240706
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.