K232732
- 510(k) number
- K232732
- Device name
- Rapid Marijuana (THC) Test Strip 20, Rapid Marijuana (THC) Test Dipcard 20, Rapid Marijuana (THC) Test Strip 50, Rapid Marijuana (THC) Test Dipcard 50
- Applicant
- Co-Innovation Biotech Co., Ltd. CN
- Product code
- LDJ — Enzyme Immunoassay, Cannabinoids
- Decision date
- 2024-01-17
- Date received
- 2023-09-07
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Clinical Toxicology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K232732.pdf
Official FDA record: K232732
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.