RecallHawk

Betel Gloves Nitrile Examination Glove Powder Free

Betel Care Sdn. Bhd.

Summary

Betel Care Sdn. Bhd. received 510(k) clearance for Betel Gloves Nitrile Examination Glove Powder Free, a LZA device. Cleared on 2022-09-24.

Details

Source

510(k) Clearance

External ID

K222342

Action Date

2022-09-24

Status

Traditional

Category

device

Product Code

LZA

Product Description

Betel Gloves Nitrile Examination Glove Powder Free. 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.

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 Betel Care Sdn. Bhd. have FDA actions?

This is the only FDA action we have on record for Betel Care Sdn. Bhd. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K222342" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for device

Related Actions