Medical Device Manufacturer · US , Ne , MN

Sonowand AS - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2009
2
Total
2
Cleared
0
Denied

Sonowand AS has 2 FDA 510(k) cleared medical devices. Based in Ne, US.

Historical record: 2 cleared submissions from 2009 to 2012. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Sonowand AS Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Sonowand AS

2 devices
1-2 of 2
Cleared Mar 23, 2012
GENERAL PRUPOSE LOCALIZERS AND ADAPTERS-NEW ACCESSORIES FOR SONOWAND SYSTEM
K112469 · HAW
Neurology · 210d
Cleared Sep 25, 2009
SONOWAND INVITE
K083597 · HAW
Neurology · 294d
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