510(k) K862153 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
ARROW 18GA TWO-LUMEN INTRAVENOUS CATH/23GA NEEDLE
| Applicant | Arrow Intl., Inc., Reading PA, US |
| Decision | Substantially Equivalent, Dec 11, 1986 |
| Received | Jun 5, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862153
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.