Medical Device Manufacturer · US , Seattle , WA

Vertis Neuroscience, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2001
2
Total
2
Cleared
0
Denied

Vertis Neuroscience, Inc. has 2 FDA 510(k) cleared medical devices. Based in Seattle, US.

Historical record: 2 cleared submissions from 2001 to 2002. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Vertis Neuroscience, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Vertis Neuroscience, Inc.

2 devices
1-2 of 2
Cleared Sep 11, 2002
VERTIS PNT CONTROL UNIT, MODEL CU 100
K022241 · NHI
Neurology · 62d
Cleared Dec 21, 2001
VERTIS PNT CONTROL UNIT, VERTIS PNT SAFEGUIDE KIDS, MODELS CU100, SGXXX
K011702 · NHI
Neurology · 203d
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