510(k) K123334 ยท DYB Introducer, Catheter
REPROCESSED STEERABLE INTRODUCER
| Applicant | Stryker Sustainability Solutions, Inc., Phoenix AZ, US |
| Decision | Substantially Equivalent, Jan 24, 2013 |
| Received | Oct 26, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123334
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.