NON-STERILE PATIENT EXAMINATION GLOVES— 510(k) K892302

Substantially Equivalent

Yeou-Fwu Rubber Industrial Co., Ltd.

FDA 510(k) clearance K892302 for NON-STERILE PATIENT EXAMINATION GLOVES, Substantially Equivalent on 1989-04-28. Applicant: Yeou-Fwu Rubber Industrial Co., Ltd.. Device class: 1.

Clearance details

Applicant
Yeou-Fwu Rubber 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
Shiang,Chang Huahsie, TW
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