510(k) K043605 ยท KNQ Dilator, Esophageal
INSCOPE 3-STAGE BALLOON DILATOR
| Applicant | Cordis Europa, N.V., Roden, Drenthe, NL |
| Decision | Substantially Equivalent, Feb 4, 2005 |
| Received | Dec 30, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K043605
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.