510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K193480Substantially Equivalent

BIOEASY Multi-Drug Test Cup

Shenzhen Bioeasy Biotechnology Co., Ltd., Shenzhen, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K193480 is the FDA 510(k) clearance record for BIOEASY Multi-Drug Test Cup, a class II device, cleared for Shenzhen Bioeasy Biotechnology Co., Ltd. on under FDA product code NGL (Test, Opiates, Over The Counter). FDA records list 5 510(k) clearances for Shenzhen Bioeasy Biotechnology Co., Ltd., from to . As of , FDA records show no recalls naming K193480.

Clearance record

Decision date
Received
(46 days to decision)
Product code
NGL Test, Opiates, Over The Counter
Regulation
21 CFR 862.3650
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Shenzhen Bioeasy Biotechnology Co., Ltd. #2-1,Liuxian 1st Rd.,Xin'An Sub-District, Shenzhen, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NGL

Trailing 12 months
1 clearance under product code NGL in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code NGL, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260