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510(k) K903654

Device
LISS CRANIAL STIMULATOR MODEL SBL202-B
Applicant
MEDICAL CONSULTANTS INTL. LTD.
510(k) number
K903654
Product code
JXK  
Decision
Substantially Equivalent (SESE)
Decision date
1990-10-04
Date received
1990-07-06
Regulation
882.5800
Classification name
Cranial Electrotherapy Stimulator To Treat Depression
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
SAUL LISS
Address
59 Oxford Pl. Glen Rock NJ US 07452 07452

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Legacy Summary#

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FDA Review#

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