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FDA 510(k)

Entarik Feeding Tube System; Entarik Feeding Tube

K-Number: K230206 · 2023-03-24

ApplicantGravitas Medical, Inc.
Decision Date2023-03-24
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Entarik Feeding Tube System; Entarik Feeding Tube is a medical device manufactured by Gravitas Medical, Inc.. It received FDA 510(k) clearance on 2023-03-24 under approval number K230206. 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 Feeding Tube System; Entarik Feeding Tube?

Entarik Feeding Tube System; Entarik Feeding Tube is a medical device that received FDA 510(k) clearance on 2023-03-24. It is manufactured by Gravitas Medical, Inc.. The 510(k) number is K230206.

When was Entarik Feeding Tube System; Entarik Feeding Tube approved by the FDA?

Entarik Feeding Tube System; Entarik Feeding Tube received FDA 510(k) clearance on 2023-03-24, under approval number K230206.

What company makes Entarik Feeding Tube System; Entarik Feeding Tube?

Entarik Feeding Tube System; Entarik Feeding Tube is manufactured by Gravitas Medical, Inc..

What is the FDA product code for Entarik Feeding Tube System; Entarik Feeding Tube?

The FDA product code for Entarik Feeding Tube System; Entarik Feeding Tube is KNT.

Other Devices by Gravitas Medical, Inc.

K241169Entarik NI Feeding Tube System

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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.

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