510(k) K830448 ยท FPA Set, Administration, Intravascular
SECURA SET VOLUME LIMITING SET
| Applicant | Diatek, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 25, 1983 |
| Received | Feb 15, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830448
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.