510(k) K053248 ยท BYI Percussor, Powered-Electric
SMARTVEST AIRWAY CLEARANCE SYSTEM, MODEL TL
| Applicant | Electromed, Inc., Mahtomedi MN, US |
| Decision | Substantially Equivalent, Dec 1, 2005 |
| Received | Nov 21, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K053248
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.