510(k) K903840 ยท DYB Introducer, Catheter
GIANT LUMEN SAFETIP SERIES: ENDOMYOCARDIAL BIOPSY
| Applicant | Intec Medical, Inc., Danvers MA, US |
| Decision | Substantially Equivalent, Oct 16, 1990 |
| Received | Aug 21, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903840
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.