Entarik NI Feeding Tube System
K-Number: K241169 · 2024-11-22
ApplicantGravitas Medical, Inc.
Decision Date2024-11-22
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Entarik NI Feeding Tube System is a medical device manufactured by Gravitas Medical, Inc.. It received FDA 510(k) clearance on 2024-11-22 under approval number K241169. 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 Entarik NI Feeding Tube System?
Entarik NI Feeding Tube System is a medical device that received FDA 510(k) clearance on 2024-11-22. It is manufactured by Gravitas Medical, Inc.. The 510(k) number is K241169.
When was Entarik NI Feeding Tube System approved by the FDA?
Entarik NI Feeding Tube System received FDA 510(k) clearance on 2024-11-22, under approval number K241169.
What company makes Entarik NI Feeding Tube System?
Entarik NI Feeding Tube System is manufactured by Gravitas Medical, Inc..
What is the FDA product code for Entarik NI Feeding Tube System?
The FDA product code for Entarik NI Feeding Tube System is KNT.
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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.