510(k) K972572 ยท DXE Catheter, Embolectomy
SINGLE LUMEN EMBOLECTOMY CATHETER
| Applicant | American Biomed, Inc., Houston TX, US |
| Decision | Substantially Equivalent, Jan 13, 1998 |
| Received | Jul 10, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972572
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.