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

Test, Cannabinoid, Over The Counter

21 CFR 862.3870 / Clinical Toxicology
FDA source (opens on fda.gov)

NFW is the FDA product code for Test, Cannabinoid, Over The Counter, a class II device type, regulated under 21 CFR 862.3870. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
NFW
Device name
Test, Cannabinoid, Over The Counter
Regulation
21 CFR 862.3870
Device class
Class II
Review panel
Clinical Toxicology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
4
Ingested recalls
0

Clearances, product code NFW

By decision year
4 clearances under product code NFW with a decision year between 2019 and 2026, 2019 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code NFW by decision year
YearClearances
20192
20231
20261

Applicants with the most clearances

Product code NFW
Applicants holding the most 510(k) clearances under product code NFW
ApplicantClearances
Healgen Scientific LLC1
Safecare Biotech(hangzhou)co.,Ltd1
Shenzhen Bioeasy Biotechnology Co., Ltd.1
Vivachek Biotech (Hangzhou) Co., Ltd1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 51 companies shown, in name order