510(k) K863684 ยท DQY Catheter, Percutaneous
URESIL SUBCLAVIAN CATHETER
| Applicant | Uresil Corp., Skokie IL, US |
| Decision | Substantially Equivalent, Jan 6, 1987 |
| Received | Sep 19, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863684
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.