Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Product codes
POP
Product code POP
Device name
Cranial Motion Measurement Device
Medical specialty
Neurology
Device class
2
Regulation number
882.1630
Review panel
NE
Implant
N
Life sustaining/supporting
N
GMP exempt
N
Third party review
Y
Summary malfunction reporting
Eligible
Definition
A cranial motion measurement device is a prescription device that utilizes accelerometers to measure the motion or acceleration of the skull. These measurements are not to be used for diagnostic purposes.
Source
FDA openFDA device classification dataset
Related 510(k) Records
#
510(k), Device, Applicant table
510(k)
Device
Applicant
Decision date
K170926
BrainPulse 1100
Jan Medical, Inc.
2017-04-28
DEN140040
Nautilus BrainPulse 1000
Jan Medical, Inc.
2016-08-01