510(k) K982889 ยท BYI Percussor, Powered-Electric
MEDPULSE RESPIRATORY VEST SYSTEM, MODEL 1000
| Applicant | Electromed, Inc., Minnetonka MN, US |
| Decision | Substantially Equivalent, Jun 1, 1999 |
| Received | Aug 17, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982889
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.