PATIENT EXAMINATION GLOVES (NATURAL RUBBER)— 510(k) K892680

Substantially Equivalent

Texla Industries Sdn. Bhd.

FDA 510(k) clearance K892680 for PATIENT EXAMINATION GLOVES (NATURAL RUBBER), Substantially Equivalent on 1989-07-14. Applicant: Texla Industries Sdn. Bhd.. Device class: 1.

Clearance details

Applicant
Texla 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
Kepong, Kuala Lumpur, MY
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