GastriSail Gastric Positioning System

FDA 510(k) K143088 · Covidien

Substantially Equivalent

510(k) numberK143088

Submission

Device name
GastriSail Gastric Positioning System
Applicant
Covidien
North Haven, CT, US
Received
October 28, 2014
Decision date
February 25, 2015
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KNT – Tubes, Gastrointestinal (And Accessories)
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5980
Specialty
Gastroenterology, Urology

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Questions and answers

When was GastriSail Gastric Positioning System cleared by the FDA?

GastriSail Gastric Positioning System (K143088) received a 510(k) decision of Substantially Equivalent on February 25, 2015, 120 days after the submission was received.

What is the product code of K143088?

The FDA product code is KNT – Tubes, Gastrointestinal (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 876.5980.