Single-Use Video Flexible Cystoscope (RP-U-C0201/RP-U-C0201S)
K-Number: K240663 · 2024-06-21
Device Summary
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.
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.