510(k) K780558 ยท BYO Bottle, Blow
BOTTLE BREATHING DEVICE
| Applicant | B & F Medical Products, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 26, 1978 |
| Received | Apr 5, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780558
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.