510(k) K961992 ยท DXE Catheter, Embolectomy
NEEDLE'S EYE SNARE
| Applicant | Cook Pacemaker Corp., Leechburg PA, US |
| Decision | Substantially Equivalent, Dec 27, 1996 |
| Received | May 21, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961992
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.