510(k) K023907 ยท KNQ Dilator, Esophageal
CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION CATHETER, CORDIS MAXI LD PTA BALLOON DILATION CATHETER
| Applicant | Cordis Corp., Warren NJ, US |
| Decision | Substantially Equivalent, Dec 18, 2002 |
| Received | Nov 25, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K023907
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.