K230281
- 510(k) number
- K230281
- Device name
- PICOCLAMP
- Applicant
- Kono Seisakusho Co., Ltd. JP
- Product code
- DXC — Clamp, Vascular
- Decision date
- 2023-10-23
- Date received
- 2023-02-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.4 MB · U.S. public domain
Also available from FDA: K230281.pdf
Official FDA record: K230281
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.