RecallHawk

InnoCare Specialty Foley Catheter

Innocare Urologics, LLC

Summary

Innocare Urologics, LLC received 510(k) clearance for InnoCare Specialty Foley Catheter, a EZL device. Cleared on 2024-09-18.

Details

Source

510(k) Clearance

External ID

K241424

Action Date

2024-09-18

Status

Traditional

Category

device

Product Code

EZL

Product Description

InnoCare Specialty Foley Catheter. Product code: EZL.

Context & Analysis

A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 389 device clearances issued this month.

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 Innocare Urologics, LLC have FDA actions?

This is the only FDA action we have on record for Innocare Urologics, LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K241424" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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