PREPOWDER VINYL PATIENT EXAMINATION GLOVES— 510(k) K962026

Name: FDA 510(k) clearance K962026
Creator: U.S. Food and Drug Administration
Published: 1996-09-10

Substantially Equivalent

Hong Huang Tang Industrial Co., Ltd.

FDA 510(k) clearance K962026 for PREPOWDER VINYL PATIENT EXAMINATION GLOVES, Substantially Equivalent on 1996-09-10. Applicant: Hong Huang Tang Industrial Co., Ltd.. Device class: 1.

Clearance details

Applicant: Hong Huang Tang Industrial Co., Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1996-05-23
Decision date: 1996-09-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Billerica, MA, US

Download summary PDF View on FDA.gov ↗

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