510(k) K000598 ยท DQY Catheter, Percutaneous
5F GUIDING CATHETER
| Applicant | Guidant Corp., Santa Clara CA, US |
| Decision | Substantially Equivalent, Mar 24, 2000 |
| Received | Feb 23, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K000598
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.