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FDA 510(k)

Sterile and Non-Sterile Ultrasonic Coupling Agent

K-Number: K242167 · 2024-09-19

ApplicantAnhui Deepblue Medical Technology Co., Ltd.
Decision Date2024-09-19
Product CodeMUI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Sterile and Non-Sterile Ultrasonic Coupling Agent is a medical device manufactured by Anhui Deepblue Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-09-19 under approval number K242167. The device is classified under product code MUI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Sterile and Non-Sterile Ultrasonic Coupling Agent?

Sterile and Non-Sterile Ultrasonic Coupling Agent is a medical device that received FDA 510(k) clearance on 2024-09-19. It is manufactured by Anhui Deepblue Medical Technology Co., Ltd.. The 510(k) number is K242167.

When was Sterile and Non-Sterile Ultrasonic Coupling Agent approved by the FDA?

Sterile and Non-Sterile Ultrasonic Coupling Agent received FDA 510(k) clearance on 2024-09-19, under approval number K242167.

What company makes Sterile and Non-Sterile Ultrasonic Coupling Agent?

Sterile and Non-Sterile Ultrasonic Coupling Agent is manufactured by Anhui Deepblue Medical Technology Co., Ltd..

What is the FDA product code for Sterile and Non-Sterile Ultrasonic Coupling Agent?

The FDA product code for Sterile and Non-Sterile Ultrasonic Coupling Agent is MUI.

Other Devices by Anhui Deepblue Medical Technology Co., Ltd.

K240242HCG Home Use Pregnancy Test Strip (Colloidal Gold), HCG Home Use Pregnancy Test Cassette (Colloidal Gold), HCG Home Use Pregnancy Test Midstream (Colloidal Gold)

Related Devices (Code: MUI)

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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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