PATIENT EXAMINATION GLOVES (LATEX)— 510(k) K892270

Substantially Equivalent

Global Latex Products Sdn Bhd

FDA 510(k) clearance K892270 for PATIENT EXAMINATION GLOVES (LATEX), Substantially Equivalent on 1989-07-14. Applicant: Global Latex Products Sdn Bhd. Device class: 1.

Clearance details

Applicant
Global Latex Products Sdn Bhd
Product code
Code LYY
Device class
Class 1
Regulation
21 CFR 880.6250
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Petaling Jaya Selang, MY
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