510(k) K024309 ยท BYI Percussor, Powered-Electric
THE VEST AIRWAY CLEARANCE SYSTEM, MODEL 104
| Applicant | Advanced Respiratory, St. Paul MN, US |
| Decision | Substantially Equivalent, Feb 21, 2003 |
| Received | Dec 24, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K024309
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.