PATIENT EXAMINATION GLOVES (LATEX)— 510(k) K892287

Name: FDA 510(k) clearance K892287
Creator: U.S. Food and Drug Administration
Published: 1990-01-10

Substantially Equivalent

Supermax Sdn Bhd

FDA 510(k) clearance K892287 for PATIENT EXAMINATION GLOVES (LATEX), Substantially Equivalent on 1990-01-10. Applicant: Supermax Sdn Bhd. Device class: 1.

Clearance details

Applicant: Supermax Sdn Bhd
Product code: Code LYY
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1989-04-06
Decision date: 1990-01-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Petaling Jaya, Selangor, 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.