Leonhard Lang Co. is one of 7708 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Leonhard Lang Co. - FDA 510(k) Cleared Devices
Recent clearances: SKINTACT ECG ELECTRODES, S&W ECG ELECTRODES
2
Total
2
Cleared
0
Denied
Leonhard Lang Co. has 2 FDA 510(k) cleared medical devices. Based in Stillwater, US.
Historical record: 2 cleared submissions from 1999 to 2003. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Leonhard Lang Co. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Product Service, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Leonhard Lang Co.
2 devices