510(k) K032138 ยท KLA Monitor, Esophageal Motility, Anorectal Motility, And Tube
MEDTRONIC SINGLE USE ESOPHAGEAL MANOMETRIC CATHETER, MEDTRONIC SINGLE USE ANORECTAL MANOMETRIC CATHETER
| Applicant | Medtronic Vascular, Shoreview MN, US |
| Decision | Substantially Equivalent, Oct 9, 2003 |
| Received | Jul 11, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032138
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.