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510(k) K841497

Device
Neuropack 8 Mee 4108
Applicant
NIHON KOHDEN AMERICA, INC.
510(k) number
K841497
Product code
GWK
Decision
Substantially Equivalent (SESE)
Decision date
1984-06-07
Date received
1984-04-10
Regulation
882.1845
Classification name
Conditioner, Signal, Physiological
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
90 Icon St. Foothill CA US 92610 92610

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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