Panasonic Corporation (Panasonic) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Panasonic Corporation (Panasonic) - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Panasonic Corporation (Panasonic) has 2 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 2 cleared submissions from 1999 to 1999. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Panasonic Corporation (Panasonic) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Panasonic Corporation (Panasonic)
2 devices