510(k) K031617 ยท KLA Monitor, Esophageal Motility, Anorectal Motility, And Tube
MEDIPLUS SINGLE USE LOWER GI MANOMETRY CATHETER
| Applicant | Mediplus , Ltd., Potomac MD, US |
| Decision | Substantially Equivalent, Jan 16, 2004 |
| Received | May 23, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031617
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.