510(k) K013202 ยท DYB Introducer, Catheter
MODIFICATION TO BRAIDED GUIDING INTRODUCER
| Applicant | Thomas Medical Products, Inc., Malvern PA, US |
| Decision | Substantially Equivalent, Oct 23, 2001 |
| Received | Sep 25, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K013202
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.