510(k) K990805 ยท QEZ Aspiration Thrombectomy Catheter
MODIFICATION TO 7F HYDROLYSER THROMBECTOMY CATHETER
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Mar 15, 1999 |
| Received | Mar 11, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K990805
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.