Atlas FDA

BIOEASY Marijuana Test Dip Card, BIOEASY Marijuana Test Strip

FDA 510(k) clearance K192301 · decided 2019-09-20

Clearance details

K-number
K192301
Device name
BIOEASY Marijuana Test Dip Card, BIOEASY Marijuana Test Strip
Applicant
Shenzhen Bioeasy Biotechnology Co., Ltd.
Decision
Substantially Equivalent
Date received
2019-08-23
Decision date
2019-09-20
Days to decision
28 days
Clearance type
Traditional
Product code
NFW
Device class
2
Regulation number
862.3870
Medical specialty
Clinical Toxicology
Advisory committee
Clinical Toxicology
Location
Shenzhen, CN
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Healgen® Accurate Oral Fluid Drug Test COT/THC; Healgen® Accurate Oral Fluid Drug Test (K252523)Healgen Scientific,, LLC2026-02-12
BioSieve™ Marijuana Test Panel 50; BioSieve™ Marijuana Test Strip 50; BioSieve™ Dx Marijuana Test Strip 20; BioSieve™ Dx Marijuana Test Strip 50; BioSieve™ Dx Marijuana Test Panel 20; BioSieve™ Dx Marijuana Test Panel 50 (K231978)Vivachek Biotech (Hangzhou) Co., Ltd.2023-08-31
SAFECARE® THC Urine Strip Test (K191924)Safecare Biotech (Hangzhou) Co., Ltd.2019-08-16

Recalls involving this device

No recalls on record reference this clearance.