510(k) K241091 ยท SDT Intra-Pulmonary Percussive Vibration (Ipv) Devices
SIMEOX 200 Airway Clearance Device
| Applicant | Inogen, Inc., Goleta CA, US |
| Decision | Substantially Equivalent, Dec 23, 2024 |
| Received | Apr 22, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241091
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.