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.. Device class: 2.

Clearance details

Applicant
Shenzhen Bioeasy Biotechnology Co., Ltd.
Product code
Code NGL
Device class
Class 2
Regulation
21 CFR 862.3650
Advisory panel
Clinical Toxicology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Shenzhen, CN
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