Entarik NI Feeding Tube System
K-Number: K241169 · 2024-11-22
Device Summary
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. The listed applicant is Gravitas Medical, Inc.. The 510(k) number is K241169.
When did Entarik NI Feeding Tube System receive FDA 510(k) clearance?
Entarik NI Feeding Tube System received FDA 510(k) clearance on 2024-11-22, under 510(k) number K241169.
Who is the listed applicant for Entarik NI Feeding Tube System?
The FDA 510(k) record lists Gravitas Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Entarik NI Feeding Tube System?
The FDA product code for Entarik NI Feeding Tube System is KNT.
Other records listing Gravitas Medical, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KNT)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.