Medical Device Manufacturer · US , Danvers , MA

Neurologica Corporation - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2005
8
Total
8
Cleared
0
Denied

FDA 510(k) cleared devices by Neurologica Corporation Radiology ✕

8 devices
1-8 of 8
Cleared Sep 08, 2025
OmniTom Elite with PCD
K250928 · JAK
Radiology · 164d
Cleared Jun 10, 2024
OmniTom Elite
K233767 · JAK
Radiology · 199d
Cleared Apr 29, 2022
BodyTom 64
K213649 · JAK
Radiology · 161d
Cleared Aug 18, 2017
OmniTom
K171183 · JAK
Radiology · 116d
Cleared Dec 23, 2014
NExCT 7
K142697 · JAK
Radiology · 92d
Cleared Mar 24, 2011
BODYTOM NL 4000
K102677 · JAK
Radiology · 190d
Cleared Aug 27, 2009
INSPIRA HD, MODEL: NL1000
K090811 · KPS
Radiology · 155d
Cleared Jul 14, 2005
CERETOM, MODEL NL3000
K051765 · JAK
Radiology · 14d
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