510(k) K926293 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
ANGIOCOR SIDEHOLE INFUSION CATHETER
| Applicant | Angiocor, Great Neck NY, US |
| Decision | Substantially Equivalent, Mar 7, 1994 |
| Received | Dec 14, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926293
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.