PATIENT EXAMINATION GLOVE (VINYL)— 510(k) K892565

Name: FDA 510(k) clearance K892565
Creator: U.S. Food and Drug Administration
Published: 1989-08-09

Substantially Equivalent

Kao Ying Industrial Co., Ltd.

FDA 510(k) clearance K892565 for PATIENT EXAMINATION GLOVE (VINYL), Substantially Equivalent on 1989-08-09. Applicant: Kao Ying Industrial Co., Ltd.. Device class: 1.

Clearance details

Applicant: Kao Ying Industrial Co., Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1989-04-13
Decision date: 1989-08-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hsien, Taiwan R.O.C., TW

Download summary PDF View on FDA.gov ↗

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