510(k) K053019 ยท DRB Stylet, Catheter
ACUITY STEERABLE STYLET ACCESSORY
| Applicant | Guidant Corporation, St Paul MN, US |
| Decision | Substantially Equivalent, Mar 3, 2006 |
| Received | Oct 26, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K053019
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.