PATIENT EXAMINATION GLOVES (VINYL)— 510(k) K891379

Name: FDA 510(k) clearance K891379
Creator: U.S. Food and Drug Administration
Published: 1989-07-14

Substantially Equivalent

Lcl Taiwan & Co., Ltd.

FDA 510(k) clearance K891379 for PATIENT EXAMINATION GLOVES (VINYL), Substantially Equivalent on 1989-07-14. Applicant: Lcl Taiwan & Co., Ltd.. Device class: 1.

Clearance details

Applicant: Lcl Taiwan & Co., Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1989-03-09
Decision date: 1989-07-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taipei, Taiwan, R.O.C., TW

Download summary PDF View on FDA.gov ↗

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