510(k) K961856 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
AUTO SUTURE CHEMOSITE TUNNELER
| Applicant | United States Surgical, A Division of Tyco Healthc, Norwalk CT, US |
| Decision | Substantially Equivalent, Jul 18, 1996 |
| Received | May 14, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961856
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.