Sterile and Non-Sterile Ultrasonic Coupling Agent
Summary
Anhui Deepblue Medical Technology Co., Ltd. received 510(k) clearance for Sterile and Non-Sterile Ultrasonic Coupling Agent, a MUI device. Cleared on 2024-09-19.
Details
Source
510(k) Clearance
External ID
K242167
Action Date
2024-09-19
Status
Traditional
Category
device
Product Code
MUI
Product Description
Sterile and Non-Sterile Ultrasonic Coupling Agent. Product code: MUI.
Context & Analysis
A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Anhui Deepblue Medical Technology Co., Ltd. has received 2 total clearances in our database.
Anhui Deepblue Medical Technology Co., Ltd. has 2 FDA actions in our database, including 2 clearances.
Frequently Asked Questions
What does 510(k) clearance mean?
A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.
How often does Anhui Deepblue Medical Technology Co., Ltd. have FDA actions?
Anhui Deepblue Medical Technology Co., Ltd. has 2 FDA actions in our database, including 0 recalls and 2 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K242167" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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