TEH LOONG POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, WHITE— 510(k) K052634

Name: FDA 510(k) clearance K052634
Creator: U.S. Food and Drug Administration
Published: 2005-10-11

Substantially Equivalent

Teh Loong Corp.

FDA 510(k) clearance K052634 for TEH LOONG POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, WHITE, Substantially Equivalent on 2005-10-11. Applicant: Teh Loong Corp.. Device class: 1.

Clearance details

Applicant: Teh Loong Corp.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 2005-09-26
Decision date: 2005-10-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, US

Download summary PDF View on FDA.gov ↗

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