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

FDA 510(k) Regulatory Record - Sonowand AS Neurology ✕

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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