ABSOGEL NON-STERILE EXAMINATION GLOVES (POWDER-FREE)— 510(k) K946056

Substantially Equivalent

Ampri Rubberware Industries Sdn Bhd

FDA 510(k) clearance K946056 for ABSOGEL NON-STERILE EXAMINATION GLOVES (POWDER-FREE), Substantially Equivalent on 1995-07-20. Applicant: Ampri Rubberware Industries Sdn Bhd. Device class: 1.

Clearance details

Applicant
Ampri Rubberware Industries 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
Selangor, MY
Download summary PDFView on FDA.gov ↗

Recent devices under product code LYY

view all

More clearances from Ampri Rubberware Industries Sdn Bhd

view all

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