K223914
- 510(k) number
- K223914
- Device name
- ACTIV Cap
- Applicant
- Cleansite Medical, Inc. CA · US
- Product code
- QBP — Cap, Device Disinfectant
- Decision date
- 2024-04-05
- Date received
- 2022-12-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K223914.pdf
Official FDA record: K223914
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.