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FDA 510(k)

Single-Use Video Hysteroscope (RP-G-C24, RP-G-C0101)

K-Number: K241987 · 2024-08-02

Decision Date2024-08-02
Product CodeHIH
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Single-Use Video Hysteroscope (RP-G-C24, RP-G-C0101) is a medical device manufactured by Guangzhou Red Pine Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2024-08-02 under approval number K241987. The device is classified under product code HIH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Single-Use Video Hysteroscope (RP-G-C24, RP-G-C0101)?

Single-Use Video Hysteroscope (RP-G-C24, RP-G-C0101) is a medical device that received FDA 510(k) clearance on 2024-08-02. It is manufactured by Guangzhou Red Pine Medical Instrument Co., Ltd.. The 510(k) number is K241987.

When was Single-Use Video Hysteroscope (RP-G-C24, RP-G-C0101) approved by the FDA?

Single-Use Video Hysteroscope (RP-G-C24, RP-G-C0101) received FDA 510(k) clearance on 2024-08-02, under approval number K241987.

What company makes Single-Use Video Hysteroscope (RP-G-C24, RP-G-C0101)?

Single-Use Video Hysteroscope (RP-G-C24, RP-G-C0101) is manufactured by Guangzhou Red Pine Medical Instrument Co., Ltd..

What is the FDA product code for Single-Use Video Hysteroscope (RP-G-C24, RP-G-C0101)?

The FDA product code for Single-Use Video Hysteroscope (RP-G-C24, RP-G-C0101) is HIH.

Related Clinical Trials

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Official Source

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