RecallHawk

Entarik Feeding Tube System; Entarik Feeding Tube

Gravitas Medical, Inc.

Summary

Gravitas Medical, Inc. received 510(k) clearance for Entarik Feeding Tube System; Entarik Feeding Tube, a KNT device. Cleared on 2023-03-24.

Details

Source

510(k) Clearance

External ID

K230206

Action Date

2023-03-24

Status

Traditional

Category

device

Product Code

KNT

Product Description

Entarik Feeding Tube System; Entarik Feeding Tube. Product code: KNT.

Context & Analysis

A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Gravitas Medical, Inc. has received 2 total clearances in our database.

Gravitas Medical, Inc. has 2 FDA actions in our database, including 2 clearances.

Frequently Asked Questions

What does 510(k) clearance mean?

A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.

How often does Gravitas Medical, Inc. have FDA actions?

Gravitas Medical, Inc. has 2 FDA actions in our database, including 0 recalls and 2 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K230206" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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