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Neurology devices

192 product codes reviewed by the Neurology panel. 6,150 510(k) clearances and 1,558 recalls in the FDA data, 84% of those recalls name a 510(k).

206510(k)s in 12 months

93recalls in 12 months

1,305recalls that name a 510(k)

Active product codes, Class I

Code	Device	Class	510(k)s, 12 mo	Recalls, 12 mo
OJG	Neurological Tray	1	0	24
QEO	Light Attenuation Lenses For Migraine-Associated Light Sensitivity	1	1	0