510(k) K933364 ยท DWO Needle, Biopsy, Cardiovascular
PROMED BIOPSY NEEDLE
| Applicant | Vlv Associates, Inc., East Hanover NJ, US |
| Decision | Substantially Equivalent, Feb 15, 1994 |
| Received | Jul 9, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933364
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.