Sensi-Pro Disposable Powdered Vinyl Synthetic Examination Gloves with White Pigment Additives

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

510(k) Number

K993231 ↗

FDA Product Code

LYZ

Device Class

Class I

Regulation

21 CFR Part 880.6250

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Lightly Powdered Vinyl Synthetic Examination Gloves

  Class I

  FDA 510(k) K972104 Active Cleared 15 Aug 1997

• Syntex

  Class I

  FDA 510(k) K971360 Active Cleared 22 Dec 1997

• Sensi-Pro Disposable Powder Free Vinyl Synthetic Examination Gloves with White Pigment Additives

  Class I

  FDA 510(k) K993240 Active Cleared 27 Oct 1999

• Powdered Latex Patient Examination Gloves

  Class I

  FDA 510(k) K051913 Active Cleared 30 Sep 2005

• Poly-Med

  Class I

  FDA 510(k) K970625 Active Cleared 27 Mar 1997

• Sensi-Pro Disposable Powder Free Synthetic Vinyl Patient Examination Gloves with Beige Pigment Additives

  Class I

  FDA 510(k) K994258 Active Cleared 20 Jan 2000

See all devices from Shinemound Enterprise, Inc. →