Aquarius Low Profile Gastrostomy Feeding Tube

FDA 510(k) K132686 · Degania Silicone , Ltd.

Unknown

510(k) numberK132686

Submission

Device name
Aquarius Low Profile Gastrostomy Feeding Tube
Applicant
Degania Silicone , Ltd.
Emek Hayarden, IL
Received
August 28, 2013
Decision date
May 12, 2014
Decision
Unknown (SESK)
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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More from Degania Silicone , Ltd.

510(k)DeviceDecision
K254170Percutaneous Endoscopic Gastrostomy (PEG) KitPIF · Traditional 03/20/2026SE
K233591StylusKNT · Traditional 05/31/2024SE
K152246Aquarius Stoma Measuring DeviceKNT · Traditional 06/21/2016SE
K143378AQUARIUS Gastrostomy Replacement TubeKNT · Special 12/29/2014SE
K141753Aquarius Nasal Feeding TubePIF · Traditional 10/16/2014SE
K141631Aquarius Extension Feeding SetKNT · Special 07/28/2014SESK
K131020Temperature Sensor CatheterEZL · Special 05/09/2013SE
K122030Low Profile Gastrostomy Feeding Tube or Gastrotomey ButtonKNT · Traditional 09/05/2012SE
K103371Coude/ or TiemannEZL · Traditional 03/11/2011SE
K070124Gastrostomy Replacement Tube, Model 253KNT · Traditional 05/23/2007SE

Questions and answers

When was Aquarius Low Profile Gastrostomy Feeding Tube cleared by the FDA?

Aquarius Low Profile Gastrostomy Feeding Tube (K132686) received a 510(k) decision of Unknown on May 12, 2014, 257 days after the submission was received.

What is the product code of K132686?

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