Siris Medical is one of 22679 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Siris Medical has 1 FDA 510(k) cleared medical devices. Based in Mountain View, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Siris Medical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Cjp Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Siris Medical
1 devices