510(k) K935292 ยท DQY Catheter, Percutaneous
SCHNEIDER GUIDEZILLA SOFTIP GUIDING CATHETER
| Applicant | Boston Scientific Scimed, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Jun 10, 1994 |
| Received | Nov 2, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935292
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.