Sterile and Non-Sterile Ultrasonic Coupling Agent
K-Number: K242167 · 2024-09-19
Device Summary
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. The listed applicant is Anhui Deepblue Medical Technology Co., Ltd.. The 510(k) number is K242167.
When did Sterile and Non-Sterile Ultrasonic Coupling Agent receive FDA 510(k) clearance?
Sterile and Non-Sterile Ultrasonic Coupling Agent received FDA 510(k) clearance on 2024-09-19, under 510(k) number K242167.
Who is the listed applicant for Sterile and Non-Sterile Ultrasonic Coupling Agent?
The FDA 510(k) record lists Anhui Deepblue Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
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 records listing Anhui Deepblue Medical Technology 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: MUI)
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.