510(k) K933992 ยท KNQ Dilator, Esophageal
OLYMPUS SCLEROTHERAPY BALLOON
| Applicant | Olympus Corp., Lake Success NY, US |
| Decision | Substantially Equivalent, Dec 21, 1993 |
| Received | Aug 17, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933992
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.