510(k) K222496 ยท BYI Percussor, Powered-Electric
Electromed SmartVest Airway Clearance System
| Applicant | Electromed, Inc., New Prague MN, US |
| Decision | Substantially Equivalent, Nov 18, 2022 |
| Received | Aug 18, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K222496
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.