PATIENT EXAMINATION GLOVES W/CORN STARCH POWDER— 510(k) K893782

Substantially Equivalent

Rubberex (M) Sdn Berhad

FDA 510(k) clearance K893782 for PATIENT EXAMINATION GLOVES W/CORN STARCH POWDER, Substantially Equivalent on 1989-07-14. Applicant: Rubberex (M) Sdn Berhad. Device class: 1.

Clearance details

Applicant
Rubberex (M) Sdn Berhad
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
Perak, Malaysia, MY
Download summary PDFView on FDA.gov ↗

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