PATIENT EXAMINATION GLOVES (LATEX)— 510(k) K892031

Substantially Equivalent

Speedtech Sdn Bhd

FDA 510(k) clearance K892031 for PATIENT EXAMINATION GLOVES (LATEX), Substantially Equivalent on 1989-08-21. Applicant: Speedtech Sdn Bhd. Device class: 1.

Clearance details

Applicant
Speedtech 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 Darul Ehsan, MY
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