510(k) K060302 ยท KNQ Dilator, Esophageal
INSCOPE PRECISION BALLOON DILATOR - WIRE GUIDED
| Applicant | Cordis Europa, N.V., Roden, Drenthe, NL |
| Decision | Substantially Equivalent, Apr 11, 2006 |
| Received | Feb 6, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060302
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.