510(k) K885149 ยท DWO Needle, Biopsy, Cardiovascular
NEEDLE INSERT FOR SOFT TISSUE BIOPSY DEVICE
| Applicant | Hart Enterprises, Inc., Wyoming MI, US |
| Decision | Substantially Equivalent, Jan 26, 1989 |
| Received | Dec 15, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885149
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.