Mcube Technology Co., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mcube Technology Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: CUBEScan BioCon-1100, CUBEScan BioCon-900S, CUBEScan BioCon-1100
6
Total
6
Cleared
0
Denied
Mcube Technology Co., Ltd. has 6 FDA 510(k) cleared medical devices. Based in Flintville, US.
Historical record: 6 cleared submissions from 2009 to 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Mcube Technology Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Mcube Technology Co., Ltd.
6 devices
Cleared
Aug 19, 2020
CUBEScan BioCon-1100
Radiology
30d
Cleared
May 19, 2020
CUBEScan BioCon-900S
Radiology
57d
Cleared
Mar 27, 2020
CUBEScan BioCon-1100
Radiology
24d
Cleared
Jun 22, 2017
CUBEScan™ BioCon-900 (Bladder Volume Measurement System)
Radiology
22d
Cleared
Apr 27, 2011
CUBESCAN / BIOCON-700
Radiology
15d
Cleared
Jun 18, 2009
CUBESCAN BIOCON-500 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
27d