Entarik Feeding Tube System; Entarik Feeding Tube

FDA 510(k) K230206 · Gravitas Medical, Inc.

Substantially Equivalent

510(k) numberK230206

Submission

Device name
Entarik Feeding Tube System; Entarik Feeding Tube
Applicant
Gravitas Medical, Inc.
San Francisco, CA, US
Received
January 25, 2023
Decision date
March 24, 2023
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KNT – Tubes, Gastrointestinal (And Accessories)
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5980
Specialty
Gastroenterology, Urology

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Questions and answers

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

Entarik Feeding Tube System; Entarik Feeding Tube (K230206) received a 510(k) decision of Substantially Equivalent on March 24, 2023, 58 days after the submission was received.

What is the product code of K230206?

The FDA product code is KNT – Tubes, Gastrointestinal (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 876.5980.