510(k) K893680 ยท DXE Catheter, Embolectomy
SILICONE BI-LUMEN IRRIGATION EMBOLECTOMY CATH.
| Applicant | Cathlab Corp., Tustin CA, US |
| Decision | Substantially Equivalent, Aug 1, 1989 |
| Received | May 16, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893680
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.