510(k) K992863 ยท DRB Stylet, Catheter
LEAD STYLET,MODELS 6505,6506,6507,6508
| Applicant | Guidant Corp., St Paul MN, US |
| Decision | Substantially Equivalent, Nov 12, 1999 |
| Received | Aug 25, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992863
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.