RecallHawk

Polyisoprene Surgical Gloves Tested for Use with Chemotherapy Drugs and Low Dermatitis Potential

Ansell Healthcare Products, LLC

Summary

Ansell Healthcare Products, LLC received 510(k) clearance for Polyisoprene Surgical Gloves Tested for Use with Chemotherapy Drugs and Low Dermatitis Potential, a KGO device. Cleared on 2023-08-23.

Details

Source

510(k) Clearance

External ID

K230079

Action Date

2023-08-23

Status

Traditional

Category

device

Product Code

KGO

Product Description

Polyisoprene Surgical Gloves Tested for Use with Chemotherapy Drugs and Low Dermatitis Potential. Product code: KGO.

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. Ansell Healthcare Products, LLC has received 3 total clearances in our database.

Ansell Healthcare Products, LLC has 6 FDA actions in our database, including 3 recalls and 3 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 Ansell Healthcare Products, LLC have FDA actions?

Ansell Healthcare Products, LLC has 6 FDA actions in our database, including 3 recalls and 3 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K230079" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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