510(k) K993629 ยท BYI Percussor, Powered-Electric
ABI VEST AIRWAY CLEARANCE SYSTEM
| Applicant | American Biosystems, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Jan 21, 2000 |
| Received | Oct 27, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993629
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.