510(k) K970229 ยท DYB Introducer, Catheter
ARROW TRANSSEPTAL SUPER ARROW-FLEX PERCUTANEOUS SET
| Applicant | Arrow Intl., Inc., Reading PA, US |
| Decision | Substantially Equivalent, Feb 13, 1998 |
| Received | Jan 21, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970229
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.