Capsule Surveillance Technologies, Sas /Capsule Tech, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Capsule Surveillance Technologies, Sas /Capsule Tech, Inc. - FDA 510(...
Recent clearances: Capsule Surveillance System
1
Total
1
Cleared
0
Denied
Capsule Surveillance Technologies, Sas /Capsule Tech, Inc. has 1 FDA 510(k) cleared medical devices. Based in Andover, US.
Last cleared in 2022. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Capsule Surveillance Technologies, Sas /Capsule Tech, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Capsule Surveillance Technologies, Sas /Capsule Tech, Inc.
1 devices