Medical Device Manufacturer · IN , Mysore

Skanray Technologies - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2011
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.

FDA 510(k) Regulatory Record - Skanray Technologies
2 devices
1-2 of 2
Cleared May 27, 2011
AIR TECHNIQUES HIGH FREQUENCY INTRA-ORAL X-RAY
K111330 · EHD
Radiology · 16d
Cleared Mar 18, 2011
INTRA SKAN DC
K103579 · EHD
Radiology · 102d
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