510(k) K062858 ยท DYB Introducer, Catheter
MODIFICATION TO GLIDESHEATH
| Applicant | Terumo Medical Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Oct 20, 2006 |
| Received | Sep 25, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K062858
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.