Stryker Communications is one of 5142 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stryker Communications - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Stryker Communications has 2 FDA 510(k) cleared medical devices. Based in Flower Mound, US.
Historical record: 2 cleared submissions from 2010 to 2013. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Stryker Communications Filter by specialty or product code using the sidebar.
Stryker Communications — FDA 510(k) Products and Clearance History
2 devices
Cleared
Dec 30, 2013
VISUM BLADE LED SURGICAL LIGHTING SYSTEM
General & Plastic Surgery
118d
Cleared
May 06, 2010
STRYKER SWITCHPOINT INFINITY 3 CONTROL SYSTEM, MODEL: 067-8001-000
Gastroenterology & Urology
41d