510(k) K860510 ยท BYI Percussor, Powered-Electric
NEONATE PERCUSSOR
| Applicant | Ballard Medical Products, Midvale UT, US |
| Decision | Substantially Equivalent, Feb 20, 1986 |
| Received | Feb 11, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860510
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.