Medical Device Manufacturer · US , Minnetonka , MN

Survivalink Corp. - FDA 510(k) Cleared Devices

7 submissions · 5 cleared · Since 1995

Total

Cleared

Denied

Survivalink Corp. has 5 FDA 510(k) cleared medical devices. Based in Minnetonka, US.

Historical record: 5 cleared submissions from 1995 to 2002. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Survivalink Corp. Filter by specialty or product code using the sidebar.

Survivalink Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Survivalink Corp.

7 devices

1-7 of 7