510(k) K844080 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
ARROW-GEISS PERCUTANEOUS TPN KIT
| Applicant | Arrow Intl., Inc., Reading PA, US |
| Decision | Substantially Equivalent, Apr 17, 1985 |
| Received | Oct 19, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K844080
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.