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FDA 510(k)

3D Endoscopic Fluorescence Camera System (DPM-ENDOCAM-06PF)

K-Number: K233892 · 2024-06-13

ApplicantZhuhai Dipu Medical Technology Co., Ltd.
Decision Date2024-06-13
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

3D Endoscopic Fluorescence Camera System (DPM-ENDOCAM-06PF) is a medical device manufactured by Zhuhai Dipu Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-06-13 under approval number K233892. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3D Endoscopic Fluorescence Camera System (DPM-ENDOCAM-06PF)?

3D Endoscopic Fluorescence Camera System (DPM-ENDOCAM-06PF) is a medical device that received FDA 510(k) clearance on 2024-06-13. It is manufactured by Zhuhai Dipu Medical Technology Co., Ltd.. The 510(k) number is K233892.

When was 3D Endoscopic Fluorescence Camera System (DPM-ENDOCAM-06PF) approved by the FDA?

3D Endoscopic Fluorescence Camera System (DPM-ENDOCAM-06PF) received FDA 510(k) clearance on 2024-06-13, under approval number K233892.

What company makes 3D Endoscopic Fluorescence Camera System (DPM-ENDOCAM-06PF)?

3D Endoscopic Fluorescence Camera System (DPM-ENDOCAM-06PF) is manufactured by Zhuhai Dipu Medical Technology Co., Ltd..

What is the FDA product code for 3D Endoscopic Fluorescence Camera System (DPM-ENDOCAM-06PF)?

The FDA product code for 3D Endoscopic Fluorescence Camera System (DPM-ENDOCAM-06PF) is GCJ.

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Other Devices by Zhuhai Dipu Medical Technology Co., Ltd.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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