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Non-Sterile, Powder-Free Nitrile Examination Glove Violet Blue Tested for use with Chemotherapy Drugs and Fentanyl and N

Sri Trang Gloves (Thailand) Public Company Limited

Summary

Sri Trang Gloves (Thailand) Public Company Limited received 510(k) clearance for Non-Sterile, Powder-Free Nitrile Examination Glove Violet Blue Tested for use with Chemotherapy Drugs and Fentanyl and Non-Sterile, Powder-Free Nitrile Examination Glove Blue Tested for use with Chemotherapy Drugs and Fentanyl, a LZA device. Cleared on 2022-11-20.

Details

Source

510(k) Clearance

External ID

K221165

Action Date

2022-11-20

Status

Abbreviated

Category

device

Product Code

LZA

Product Description

Non-Sterile, Powder-Free Nitrile Examination Glove Violet Blue Tested for use with Chemotherapy Drugs and Fentanyl and Non-Sterile, Powder-Free Nitrile Examination Glove Blue Tested for use with Chemotherapy Drugs and Fentanyl. Product code: LZA.

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. Sri Trang Gloves (Thailand) Public Company Limited has received 5 total clearances in our database.

Sri Trang Gloves (Thailand) Public Company Limited has 5 FDA actions in our database, including 5 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 Sri Trang Gloves (Thailand) Public Company Limited have FDA actions?

Sri Trang Gloves (Thailand) Public Company Limited has 5 FDA actions in our database, including 0 recalls and 5 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K221165" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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