510(k) K080303 ยท FPA Set, Administration, Intravascular
EZ REGULAR
| Applicant | Meinntech Co., Ltd., Deer Field IL, US |
| Decision | Substantially Equivalent, Aug 5, 2008 |
| Received | Feb 5, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080303
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.