510(k) K142000 ยท PIE Esophageal Dilator With Balloon And Electrode Sensors
ESOFLIP ES
| Applicant | Crospon, Ltd., Bonita Springs FL, US |
| Decision | Substantially Equivalent, Sep 25, 2014 |
| Received | Jul 23, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142000
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.