510(k) K931988 ยท BYI Percussor, Powered-Electric
3P (PULMONARY PERCUSSIVE PACK)
| Applicant | Delta Medical Manuf, Inc., Raleigh NC, US |
| Decision | Substantially Equivalent, Oct 28, 1994 |
| Received | Apr 22, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931988
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.