MEDTRONIC SINGLE USE ESOPHAGEAL MANOMETRIC CATHETER, MEDTRONIC SINGLE USE ANORECTAL MANOMETRIC CATHETER— 510(k) K032138

Substantially Equivalent

Medtronic Vascular

FDA 510(k) clearance K032138 for MEDTRONIC SINGLE USE ESOPHAGEAL MANOMETRIC CATHETER, MEDTRONIC SINGLE USE ANORECTAL MANOMETRIC CATHETER, Substantially Equivalent on 2003-10-09. Applicant: Medtronic Vascular. Device class: 2.

Clearance details

Applicant
Medtronic Vascular
Product code
Code KLA
Device class
Class 2
Regulation
21 CFR 876.1725
Advisory panel
Gastroenterology, Urology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Shoreview, MN, US
Download summary PDFView on FDA.gov ↗

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