K231484
- 510(k) number
- K231484
- Device name
- PureWay 1.4 Quart Sharps Collector
- Applicant
- Pureway Compliance, Inc. CA · US
- Product code
- MMK — Container, Sharps
- Decision date
- 2023-09-14
- Date received
- 2023-05-23
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K231484.pdf
Official FDA record: K231484
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.