K253303
- 510(k) number
- K253303
- Device name
- Dendrite Imaging System
- Applicant
- Dendrite Imaging, Inc. CA · US
- Product code
- QDG — Parathyroid Autofluorescence Imaging Device
- Decision date
- 2025-11-28
- Date received
- 2025-09-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K253303.pdf
Official FDA record: K253303
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.