510(k) K040367 ยท BYI Percussor, Powered-Electric
MEDPULSE RESPIRATORY VEST SYSTEM, MODEL 2000EZ
| Applicant | Electromed, Inc., New Prague MN, US |
| Decision | Substantially Equivalent, Apr 7, 2004 |
| Received | Feb 13, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K040367
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.