PATIENT EXAMINATION GLOVES (LATEX)— 510(k) K892011

Name: FDA 510(k) clearance K892011
Creator: U.S. Food and Drug Administration
Published: 1989-05-01

Substantially Equivalent

Mediglove Sdn. Bhd.

FDA 510(k) clearance K892011 for PATIENT EXAMINATION GLOVES (LATEX), Substantially Equivalent on 1989-05-01. Applicant: Mediglove Sdn. Bhd.. Device class: 1.

Clearance details

Applicant: Mediglove Sdn. Bhd.
Product code: Code LYY
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1989-03-30
Decision date: 1989-05-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kajang, Selangor Darul, MY

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.