RecallHawk

Powder Free Latex Patient Examination Glove, Black Colored, Non-sterile, with Protein Content labeling Claim (Contains 5

Kossan International Sdn Bhd

Summary

Kossan International Sdn Bhd received 510(k) clearance for Powder Free Latex Patient Examination Glove, Black Colored, Non-sterile, with Protein Content labeling Claim (Contains 50 ug per dm2 of glove or less of Total Water Extractable Protein), a LYY device. Cleared on 2023-06-13.

Details

Source

510(k) Clearance

External ID

K230573

Action Date

2023-06-13

Status

Traditional

Category

device

Product Code

LYY

Product Description

Powder Free Latex Patient Examination Glove, Black Colored, Non-sterile, with Protein Content labeling Claim (Contains 50 ug per dm2 of glove or less of Total Water Extractable Protein). Product code: LYY.

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. Kossan International Sdn Bhd has received 3 total clearances in our database.

Kossan International Sdn Bhd has 3 FDA actions in our database, including 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 Kossan International Sdn Bhd have FDA actions?

Kossan International Sdn Bhd has 3 FDA actions in our database, including 0 recalls and 3 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K230573" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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