Nitrile Powder Free Examination Glove with Tremella Fuciformis Extract, Tested for Use with Chemotherapy Drugs and Fenta
Summary
Mah Sing Healthcare Sdn. Bhd. received 510(k) clearance for Nitrile Powder Free Examination Glove with Tremella Fuciformis Extract, Tested for Use with Chemotherapy Drugs and Fentanyl Citrate - Blue, a LZA device. Cleared on 2025-06-06.
Details
Source
510(k) Clearance
External ID
K243694
Action Date
2025-06-06
Status
Traditional
Category
device
Product Code
LZA
Product Description
Nitrile Powder Free Examination Glove with Tremella Fuciformis Extract, Tested for Use with Chemotherapy Drugs and Fentanyl Citrate - Blue. 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. Mah Sing Healthcare Sdn. Bhd. has received 5 total clearances in our database.
Mah Sing Healthcare Sdn. Bhd. 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 Mah Sing Healthcare Sdn. Bhd. have FDA actions?
Mah Sing Healthcare Sdn. Bhd. 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 "K243694" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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