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)

CORGRIP* SR NG/NI Tube Retention System

K-Number: K241185 · 2024-10-25

ApplicantAvanos Medical, Inc.
Decision Date2024-10-25
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CORGRIP* SR NG/NI Tube Retention System is a medical device manufactured by Avanos Medical, Inc.. It received FDA 510(k) clearance on 2024-10-25 under approval number K241185. 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 CORGRIP* SR NG/NI Tube Retention System?

CORGRIP* SR NG/NI Tube Retention System is a medical device that received FDA 510(k) clearance on 2024-10-25. It is manufactured by Avanos Medical, Inc.. The 510(k) number is K241185.

When was CORGRIP* SR NG/NI Tube Retention System approved by the FDA?

CORGRIP* SR NG/NI Tube Retention System received FDA 510(k) clearance on 2024-10-25, under approval number K241185.

What company makes CORGRIP* SR NG/NI Tube Retention System?

CORGRIP* SR NG/NI Tube Retention System is manufactured by Avanos Medical, Inc..

What is the FDA product code for CORGRIP* SR NG/NI Tube Retention System?

The FDA product code for CORGRIP* SR NG/NI Tube Retention System is KNT.

Related Clinical Trials

NCT07382674 Zesty Exercise System for Therapeutic Engagement RECRUITING NCT05006339 The Use of Remote Monitoring for Orthodontic Retention Review ACTIVE_NOT_RECRUITING NCT04784832 TMS-based Assessment of Mental Training Effects on Motor Learning in Healthy Participants RECRUITING NCT05465161 STING MARK Universal Fiducial Marker System RECRUITING

Other Devices by Avanos Medical, Inc.

K191340CORTRAK* 2 Equilateral Enteral Access System K203066COOLIEF Cooled Radiofrequency Kit Advanced K192491Coolief Radiofrequency Generator (CRG) System K220588Avanos* CORTRAK* 2 Enteral Access System (EAS) K242057COOLIEF* Radiofrequency Generator (CRG-BASIC, CRG-BASIC-R, CRG-ADVANCED, CRG-ADVANCED-R) K240965CORTRAK* 2 Enteral Access System (20-0950)

View all 8 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.

↑