PATIENT EXAMINATION GLOVES (LATEX)— 510(k) K892737

Substantially Equivalent

Kds Latex Industrial Co., Ltd.

FDA 510(k) clearance K892737 for PATIENT EXAMINATION GLOVES (LATEX), Substantially Equivalent on 1989-05-11. Applicant: Kds Latex Industrial Co., Ltd.. Device class: 1.

Clearance details

Applicant
Kds Latex Industrial Co., Ltd.
Product code
Code LYY
Device class
Class 1
Regulation
21 CFR 880.6250
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Taichung City, TW
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