Tyco Electronics Corporation is one of 22251 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tyco Electronics Corporation - FDA 510(k) Cleared Devices
Recent clearances: TYCO ELECTRONICS ELECTROCARDIOGRAPH (ECG) LEADWIRE SET
1
Total
1
Cleared
0
Denied
Tyco Electronics Corporation has 1 FDA 510(k) cleared medical devices. Based in Wilsonville, US.
Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Tyco Electronics Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Sud America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Tyco Electronics Corporation
1 devices