510(k) K926038 ยท KNQ Dilator, Esophageal
FLEX-TECH BALLOON DILATOR
| Applicant | Cape Tech Medical Products, Falmouth MA, US |
| Decision | Substantially Equivalent, Oct 25, 1993 |
| Received | Dec 1, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926038
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.