510(k) K961999 ยท DYG Catheter, Flow Directed
SCHNEIDER GUIDER SOFTIP GUIDING CATHETERS
| Applicant | Boston Scientific Scimed, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Nov 19, 1996 |
| Received | May 22, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961999
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.