Skanray Technologies is one of 163 FDA 510(k) medical device manufacturers from India in the dataset, ranked by real submission volume.
Skanray Technologies - FDA 510(k) Cleared Devices
Recent clearances: AIR TECHNIQUES HIGH FREQUENCY INTRA-ORAL X-RAY, INTRA SKAN DC
2
Total
2
Cleared
0
Denied
Skanray Technologies has 2 FDA 510(k) cleared medical devices. Based in Mysore, IN.
Historical record: 2 cleared submissions from 2011 to 2011. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Skanray Technologies Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Skanray Technologies
2 devices