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FDA 510(k)

Single-Use Video Flexible Cystoscope (RP-U-C0201/RP-U-C0201S)

K-Number: K240663 · 2024-06-21

Decision Date2024-06-21
Product CodeFAJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Single-Use Video Flexible Cystoscope (RP-U-C0201/RP-U-C0201S) is a medical device manufactured by Guangzhou Red Pine Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2024-06-21 under approval number K240663. The device is classified under product code FAJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Single-Use Video Flexible Cystoscope (RP-U-C0201/RP-U-C0201S)?

Single-Use Video Flexible Cystoscope (RP-U-C0201/RP-U-C0201S) is a medical device that received FDA 510(k) clearance on 2024-06-21. It is manufactured by Guangzhou Red Pine Medical Instrument Co., Ltd.. The 510(k) number is K240663.

When was Single-Use Video Flexible Cystoscope (RP-U-C0201/RP-U-C0201S) approved by the FDA?

Single-Use Video Flexible Cystoscope (RP-U-C0201/RP-U-C0201S) received FDA 510(k) clearance on 2024-06-21, under approval number K240663.

What company makes Single-Use Video Flexible Cystoscope (RP-U-C0201/RP-U-C0201S)?

Single-Use Video Flexible Cystoscope (RP-U-C0201/RP-U-C0201S) is manufactured by Guangzhou Red Pine Medical Instrument Co., Ltd..

What is the FDA product code for Single-Use Video Flexible Cystoscope (RP-U-C0201/RP-U-C0201S)?

The FDA product code for Single-Use Video Flexible Cystoscope (RP-U-C0201/RP-U-C0201S) is FAJ.

Related Clinical Trials

Other Devices by Guangzhou Red Pine Medical Instrument Co., Ltd.

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Related Devices (Code: FAJ)

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.