HONYEE VINYL EXAMINATION GLOVES— 510(k) K893822

Name: FDA 510(k) clearance K893822
Creator: U.S. Food and Drug Administration
Published: 1989-08-22

Substantially Equivalent

Honyee Enterprise Co.

FDA 510(k) clearance K893822 for HONYEE VINYL EXAMINATION GLOVES, Substantially Equivalent on 1989-08-22. Applicant: Honyee Enterprise Co.. Device class: 1.

Clearance details

Applicant: Honyee Enterprise Co.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1989-05-23
Decision date: 1989-08-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tainan, TW

Download summary PDF View on FDA.gov ↗

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