510(k) K924541 ยท BYO Bottle, Blow
EPIDURAL MINIPACK
| Applicant | Concord/Portex, Keene NH, US |
| Decision | Unknown, Jul 9, 1993 |
| Received | Sep 8, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924541
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.