510(k) K954798 ยท KLA Monitor, Esophageal Motility, Anorectal Motility, And Tube
7100 SWALLOWING WORKSTATION
| Applicant | Kay Elemetrics Corp., Lincoln Park NJ, US |
| Decision | Substantially Equivalent, Jun 4, 1996 |
| Received | Oct 18, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954798
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.