510(k) K862000 ยท KNQ Dilator, Esophageal
KEYMED FLEXIBLE ESOPHAGEAL DILATORS
| Applicant | Keymed, Inc., Essex Ss2 5qh England, GB |
| Decision | Substantially Equivalent, Aug 12, 1986 |
| Received | May 23, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862000
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.