Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Micro Transgastric-Jejunal Feeding Device

K-Number: K183508 · 2019-03-29

ApplicantApplied Medical Technology, Inc.
Decision Date2019-03-29
Product CodeKNT
Advisory CommitteeGU
DecisionUnknown

Device Summary

Micro Transgastric-Jejunal Feeding Device is a medical device manufactured by Applied Medical Technology, Inc.. It received FDA 510(k) clearance on 2019-03-29 under approval number K183508. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the Micro Transgastric-Jejunal Feeding Device?

Micro Transgastric-Jejunal Feeding Device is a medical device that received FDA 510(k) clearance on 2019-03-29. It is manufactured by Applied Medical Technology, Inc.. The 510(k) number is K183508.

When was Micro Transgastric-Jejunal Feeding Device approved by the FDA?

Micro Transgastric-Jejunal Feeding Device received FDA 510(k) clearance on 2019-03-29, under approval number K183508.

What company makes Micro Transgastric-Jejunal Feeding Device?

Micro Transgastric-Jejunal Feeding Device is manufactured by Applied Medical Technology, Inc..

What is the FDA product code for Micro Transgastric-Jejunal Feeding Device?

The FDA product code for Micro Transgastric-Jejunal Feeding Device is KNT.

Related Clinical Trials

NCT05729477 A Prospective Multicenter Study To Assess The Clinical Outcomes Of Current Phacoemulsification Approach To Cataract Extraction Versus The Micor System Device TERMINATED NCT05505513 Can an Array of Micro-electrodes Implanted in a Human Nerve Record Neural Signals and Provide Feedback? RECRUITING NCT07576972 Human Milk Concentrating Device to Optimize Mother's Own Milk NOT_YET_RECRUITING NCT04092660 Increasing the Use of an Anti-snoring Mouth Guard (Mandibular Advancement Appliance) to Prevent Upper Airway Collapse During Sleep in Patients With Obstructive Sleep Apnoea. RECRUITING NCT04251377 Single-stage Surgery With Antibiotic-loaded Hydrogel Coated Implants Versus Two Stage Surgery for Secondary Prevention of Complex Chronic Periprosthetic Hip Joint Infection ACTIVE_NOT_RECRUITING NCT05335187 Hybrid Micro-macro Electrodes in Patients With Epilepsy RECRUITING

Other Devices by Applied Medical Technology, Inc.

K170319Low Profile Non-Balloon Feeding Device K161413Low Profile Balloon Feeding Device K180026Bowel Management Device, Bowel Management Irrigation Set K182804Traditional Length GJ Feeding Device K202539Nutriglide(TM) Nasal Feeding Tube K193612AMT Suture Delivery System

View all 11 devices →

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.

↑