510(k) K812151 ยท BYI Percussor, Powered-Electric
MJ NEONATAL PERCUSSOR
| Applicant | Cussionair Therapy Products, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 25, 1981 |
| Received | Jul 29, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812151
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.