K222613
- 510(k) number
- K222613
- Device name
- ARX Liquid Amies Collection & Transport System
- Applicant
- Arx Sciences, Inc. NY · US
- Product code
- LIO — Device, Specimen Collection
- Decision date
- 2024-03-27
- Date received
- 2022-08-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Microbiology
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K222613.pdf
Official FDA record: K222613
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.