510(k) K012928 ยท BYI Percussor, Powered-Electric
ABI VEST AIRWAY CLEARANCE SYSTEM
| Applicant | Advanced Respiratory, St. Paul MN, US |
| Decision | Substantially Equivalent, Oct 9, 2001 |
| Received | Aug 31, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012928
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.