HEDY PATIENT EXAMINATION GLOVES (VINYL)— 510(k) K891670

Name: FDA 510(k) clearance K891670
Creator: U.S. Food and Drug Administration
Published: 1989-10-31

Substantially Equivalent

Hedd Industry Corp.

FDA 510(k) clearance K891670 for HEDY PATIENT EXAMINATION GLOVES (VINYL), Substantially Equivalent on 1989-10-31. Applicant: Hedd Industry Corp.. Device class: 1.

Clearance details

Applicant: Hedd Industry Corp.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1989-03-20
Decision date: 1989-10-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taipei (11720), Taiwan, TW

Download summary PDF View on FDA.gov ↗

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