Stryker Communications Corp. is one of 25201 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stryker Communications Corp. - FDA 510(k) Cleared Devices
Recent clearances: VISUM LED SURGICAL LIGHTING SYSTEM, STRYKER SWITCHPOINT INFINITY
2
Total
2
Cleared
0
Denied
Stryker Communications Corp. has 2 FDA 510(k) cleared medical devices. Based in Poway, US.
Historical record: 2 cleared submissions from 2004 to 2006. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Stryker Communications Corp. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Stryker Communications Corp.
2 devices