POWDER FREE VINYL PATIENT EXAMINATION GLOVE, YELLOW— 510(k) K070188

Name: FDA 510(k) clearance K070188
Creator: U.S. Food and Drug Administration
Published: 2007-03-19

Substantially Equivalent

Hong DI Plastic Products Co., Ltd.

FDA 510(k) clearance K070188 for POWDER FREE VINYL PATIENT EXAMINATION GLOVE, YELLOW, Substantially Equivalent on 2007-03-19. Applicant: Hong DI Plastic Products Co., Ltd.. Device class: 1.

Clearance details

Applicant: Hong DI Plastic Products Co., Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 2007-01-22
Decision date: 2007-03-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chino, CA, US

Download summary PDF View on FDA.gov ↗

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