510(k) K993720 ยท KNQ Dilator, Esophageal
CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION CATHETER
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Jan 18, 2000 |
| Received | Nov 3, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993720
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.