PATIENT EXAMINATION LATEX GLOVES, HYPOALLERGENIC— 510(k) K915251

Name: FDA 510(k) clearance K915251
Creator: U.S. Food and Drug Administration
Published: 1993-01-22

Substantially Equivalent

Supermax Sdn Bhd

FDA 510(k) clearance K915251 for PATIENT EXAMINATION LATEX GLOVES, HYPOALLERGENIC, Substantially Equivalent on 1993-01-22. 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: 1991-11-13
Decision date: 1993-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Selangor, Malaysia, MG

Download summary PDF View on FDA.gov ↗

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