510(k) K132794 ยท BYI Percussor, Powered-Electric
SMARTVEST AIRWAY CLEARANCE SYSTEM
| Applicant | Electromed, Inc., New Prague MN, US |
| Decision | Substantially Equivalent, Dec 19, 2013 |
| Received | Sep 6, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K132794
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.