Single-Use Video Hysteroscope (RP-G-C24, RP-G-C0101)
K-Number: K241987 · 2024-08-02
Device Summary
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. The listed applicant is Guangzhou Red Pine Medical Instrument Co., Ltd.. The 510(k) number is K241987.
When did Single-Use Video Hysteroscope (RP-G-C24, RP-G-C0101) receive FDA 510(k) clearance?
Single-Use Video Hysteroscope (RP-G-C24, RP-G-C0101) received FDA 510(k) clearance on 2024-08-02, under 510(k) number K241987.
Who is the listed applicant for Single-Use Video Hysteroscope (RP-G-C24, RP-G-C0101)?
The FDA 510(k) record lists Guangzhou Red Pine Medical Instrument Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Guangzhou Red Pine Medical Instrument Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: HIH)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.