BIOEASY Multi-Drug Test Cup— 510(k) K193480

Substantially Equivalent

Shenzhen Bioeasy Biotechnology Co., Ltd.

FDA 510(k) clearance K193480 for BIOEASY Multi-Drug Test Cup, Substantially Equivalent on 2020-01-31. Applicant: Shenzhen Bioeasy Biotechnology Co., Ltd..

Clearance details

Applicant: Shenzhen Bioeasy Biotechnology Co., Ltd.
Product code: Code NGL
Advisory panel: Clinical Toxicology
Date received: 2019-12-16
Decision date: 2020-01-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

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