K233076
- 510(k) number
- K233076
- Device name
- Laser Speckle Imaging System (RFLSI CZW)
- Applicant
- Rwd Life Science Co., Ltd. CN
- Product code
- DPT — Probe, Blood-Flow, Extravascular
- Decision date
- 2024-05-28
- Date received
- 2023-09-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K233076.pdf
Official FDA record: K233076
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.