K233892
- 510(k) number
- K233892
- Device name
- 3D Endoscopic Fluorescence Camera System (DPM-ENDOCAM-06PF)
- Applicant
- Zhuhai Dipu Medical Technology Co., Ltd. CN
- Product code
- GCJ — Laparoscope, General & Plastic Surgery
- Decision date
- 2024-06-13
- Date received
- 2023-12-08
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K233892.pdf
Official FDA record: K233892
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.