510(k) K961895 ยท KLA Monitor, Esophageal Motility, Anorectal Motility, And Tube
FLEXILOG LS 13921
| Applicant | Oakfield Instruments, Ltd., Oxon Ox8 1ja England, GB |
| Decision | Substantially Equivalent, Nov 4, 1996 |
| Received | May 16, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961895
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.