Medical Device Manufacturer · US , Austin , TX

Intronix Technologies Corp. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2011
1
Total
1
Cleared
0
Denied

Intronix Technologies Corp. has 1 FDA 510(k) cleared medical devices. Based in Austin, US.

Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Intronix Technologies Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Intronix Technologies Corp.
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