Aspire Venting Tube
K-Number: K182248 · 2018-11-13
ApplicantAspire Bariatrics, Inc.
Decision Date2018-11-13
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Aspire Venting Tube is a medical device manufactured by Aspire Bariatrics, Inc.. It received FDA 510(k) clearance on 2018-11-13 under approval number K182248. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Aspire Venting Tube?
Aspire Venting Tube is a medical device that received FDA 510(k) clearance on 2018-11-13. It is manufactured by Aspire Bariatrics, Inc.. The 510(k) number is K182248.
When was Aspire Venting Tube approved by the FDA?
Aspire Venting Tube received FDA 510(k) clearance on 2018-11-13, under approval number K182248.
What company makes Aspire Venting Tube?
Aspire Venting Tube is manufactured by Aspire Bariatrics, Inc..
What is the FDA product code for Aspire Venting Tube?
The FDA product code for Aspire Venting Tube is KNT.
Other Devices by Aspire Bariatrics, Inc.
Related Devices (Code: KNT)
K163092TubeClear Control Box and Clearing StemActuated Medical, Inc.
K162110CORGRIP NG/NI Tube Retention SystemCorpak Medsystems, Inc. A Division of Haylard Health
K160787Gabriel Feeding Tube with Balloon, Magnetically Guided Feeding Tube w/Balloon, Gabriel Feeding Tube with Balloon, Preassembled with StyletSyncro Medical Innovations, Inc.
K152246Aquarius Stoma Measuring DeviceDegania Silicone , Ltd.
K153506Qora AIM Stool Management Kit, Qora Aeon Stool Management Kit, Qora Arida Stool Management KitConsure Medical Pvt , Ltd.
K160654GastriSail Gastric Positioning System 40 Fr/CH (13.3mm)Covidien, LLC
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.