Dermagrip Powder Free Latex Examination Glove, Non Sterile (Protein Content Labeling)

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

510(k) Number

K991044 ↗

FDA Product Code

LYY

Device Class

Class I

Regulation

21 CFR Part 880.6250

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Dermagrip Powder-Free Latex Surgical Glove, Sterile (Protein Content Labeling 50 Micrograms or Less)

  Class I

  FDA 510(k) K993214 Active Cleared 2 Dec 1999

• Dermagrip Powdered Latex Surgical Glove, Sterile

  Class I

  FDA 510(k) K993215 Active Cleared 2 Dec 1999

• Dermagrip Powder Free Latex Examination Gloves with Aloe Vera Protein Content Labeling Claim (50 Micrograms or Less)

  Class I

  FDA 510(k) K012876 Active Cleared 1 Oct 2001

• Dermagrip Powder Free Green Polymer Coated Examination Gloves Contains 50 Micrograms or Less of Total Water Extractable

  Class I

  FDA 510(k) K003309 Active Cleared 22 Nov 2000

• Dermagrip and Multiple Powder Free Purple Nitrile Examination Gloves, Non-Sterile

  Class I

  FDA 510(k) K021396 Active Cleared 16 May 2002

• Dermagrip and Multiple Powder Free Latex Examination Gloves, Sterile with Protein Content Labeling Claim (50 Microgram O

  Class I

  FDA 510(k) K021561 Active Cleared 11 Jun 2002

See all devices from Wrp Specialty Products Sdn. Bhd. →