Medi-Plus, Health-Plus, Sanitex, Reliance

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K973551 ↗

FDA Product Code

LZA

Device Class

Class I

Regulation

21 CFR Part 880.6250

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Medi-Plus, Health-Plus, Sanitex, Reliance

  Class I

  FDA 510(k) K972169 Active Cleared 3 Oct 1997

• Health-Plus, Sanitex, Reliance, Powdered Latex Exam Gloves Contains 100 Micrograms or Less of Total Water Extractable Pr

  Class I

  FDA 510(k) K001475 Active Cleared 13 Jun 2000

• Health-Plus, Sanitex, Reliance Powder-Free Nitrile Examination Gloves

  Class I

  FDA 510(k) K010077 Active Cleared 28 Feb 2001

• Medi-Plus, Health Plus, Sanitex, Reliance

  Class I

  FDA 510(k) K953138 Active Cleared 22 Sep 1995

• Powder-Free Multi-Ply Latex Examination Gloves, Polymer Coated on Outside and Nitrile Coated on Inside, Blue Color with

  Class I

  FDA 510(k) K011895 Active Cleared 9 Jul 2001

• Powder-Free Latex Examination Gloves

  Class I

  FDA 510(k) K964724 Active Cleared 16 Jun 1997

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