510(k) K983940 ยท DYB Introducer, Catheter
EZ-INTRO PERCUTANEOUS CATHETER SHEATH, EZ-INTRO VESSEL DILATOR
| Applicant | Adam Spence Corp., Wall NJ, US |
| Decision | Substantially Equivalent, Jul 15, 1999 |
| Received | Nov 5, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983940
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.