K231752
- 510(k) number
- K231752
- Device name
- ARK Hydrocodone Assay
- Applicant
- Ark Diagnostics, Inc. CA · US
- Product code
- DJG — Enzyme Immunoassay, Opiates
- Decision date
- 2023-11-09
- Date received
- 2023-06-15
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Clinical Toxicology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K231752.pdf
Official FDA record: K231752
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.