510(k) K921295 ยท FGO Dislodger, Stone, Flexible
INTRAVENOUS CATHETERS MODIFICATIONS
| Applicant | Critikon Company, LLC, Tampa FL, US |
| Decision | Substantially Equivalent, May 17, 1993 |
| Received | Mar 12, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921295
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.