510(k) K090114 ยท DYB Introducer, Catheter
MODIFICATION TO:INTRODUCER SETS, MODEL ADELANTE AND ADELANTE-S
| Applicant | Oscor, Inc., Palm Harbor FL, US |
| Decision | Substantially Equivalent, Jun 4, 2009 |
| Received | Jan 21, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K090114
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.