Brightway Brand Latex Examination Glove-(Powdered, Sterile), Containing 150 Ugm or Less of Water Extractable Protein per

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K032938 ↗

FDA Product Code

LYY

Device Class

Class I

Regulation

21 CFR Part 880.6250

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Brightway Brand Nitrile Examination Gloves 12”, Powder Free, [Purple] Tested for Use with Chemotherapy Drugs

  Class I

  FDA 510(k) K162294 Active Cleared 21 Apr 2017

• Brightway Brand Blue Nitrile Examination Gloves (Powdered)

  Class I

  FDA 510(k) K990876 Active Cleared 23 Jun 1999

• Brightway Brand Nitrile Surgical Gloves - Sterile (Powdered)

  Class I

  FDA 510(k) K991940 Active Cleared 12 Jul 1999

• Nitrile Examination Gloves, Powder Free [Purple] Tested for Use with Chemotherapy Drugs

  Class I

  FDA 510(k) K170686 Active Cleared 14 Jul 2017

• Brightway Brand Nitrile Examination Gloves 12”, Powder Free, [Sterling/Grey] with Chemotherapy Claim

  Class I

  FDA 510(k) K162186 Active Cleared 31 Mar 2017

• Brightway Brand Blue Nitrile Examination Gloves (Powder Free)

  Class I

  FDA 510(k) K990878 Active Cleared 21 May 1999

See all devices from Brightway Holdings Sdn. Bhd. →