510(k) K921418 ยท DWO Needle, Biopsy, Cardiovascular
ULTRA-CORE BIOPSY NEEDLES
| Applicant | Medical Device Technologies, Inc., Gainsville FL, US |
| Decision | Substantially Equivalent, Jun 19, 1992 |
| Received | Mar 24, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921418
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.