AMPRI— 510(k) K954002

Substantially Equivalent

Ampri Rubberware Industries Sdn Bhd

FDA 510(k) clearance K954002 for AMPRI, Substantially Equivalent on 1996-01-29. Applicant: Ampri Rubberware Industries Sdn Bhd. Device class: 1.

Clearance details

Applicant
Ampri Rubberware Industries Sdn Bhd
Product code
Code KGO
Device class
Class 1
Regulation
21 CFR 878.4460
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Selangor, MY
Download summary PDFView on FDA.gov ↗

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