Watermark Medical is one of 19099 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Watermark Medical - FDA 510(k) Cleared Devices
Recent clearances: Apnea Risk Evaluation System (ARES), Model 620, CONNECTED CARE MOBILE APPLICATION, MIPAL
3
Total
3
Cleared
0
Denied
Watermark Medical has 3 FDA 510(k) cleared medical devices. Based in Brookfield, US.
Historical record: 3 cleared submissions from 2012 to 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Watermark Medical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Michael Leigh as regulatory consultant.
FDA 510(k) Regulatory Record - Watermark Medical
3 devices