Panasonic Healthcare Co., Ltd. is one of 16435 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Panasonic Healthcare Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: AIDA VI.8 DIAGNOSTIC ULTRASOUND GM-72P00A, L13-5V1 TRANSDUCER, AIDA V1.5 DIAGNOSTIC ULTRASOUND SYSTEM GM-72P00A, AIDA DIAGNOSTIC ULTRASOUND SYSTEM
3
Total
3
Cleared
0
Denied
Panasonic Healthcare Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Issaquah, US.
Historical record: 3 cleared submissions from 2011 to 2012. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Panasonic Healthcare Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Panasonic Healthcare Co., Ltd.
3 devices