POWDER FREE (YELLOW) VINYL PATIENT EXAMINATION— 510(k) K070044

Name: FDA 510(k) clearance K070044
Creator: U.S. Food and Drug Administration
Published: 2007-01-29

Substantially Equivalent

Shijiazhuang Lianhe Shunda Plastic Products Co., L

FDA 510(k) clearance K070044 for POWDER FREE (YELLOW) VINYL PATIENT EXAMINATION, Substantially Equivalent on 2007-01-29. Applicant: Shijiazhuang Lianhe Shunda Plastic Products Co., L. Device class: 1.

Clearance details

Applicant: Shijiazhuang Lianhe Shunda Plastic Products Co., L
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 2007-01-03
Decision date: 2007-01-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chino, CA, US

Download summary PDF View on FDA.gov ↗

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K070026 — POWDERED (YELLOW) VINYL PATIENT EXAMINATION GLOVES2007-03-07
K070037 — POWDER FREE VINYL PATIENT EXAMINATION GLOVE2007-02-20
K070046 — POWDERED VINYL PATIENT GLOVE2007-02-07

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