510(k) K013704 ยท KLA Monitor, Esophageal Motility, Anorectal Motility, And Tube
MEDIPLUS SINGLE USE GI MANOMETRY CATHETER
| Applicant | Mediplus , Ltd., St. Petersburg FL, US |
| Decision | Substantially Equivalent, Aug 5, 2002 |
| Received | Nov 8, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013704
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.