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510(k) K843923

Device
THYMATRON
Applicant
SOMATICS, INC.
510(k) number
K843923
Product code
GXC  
Decision
Substantially Equivalent (SESE)
Decision date
1984-12-03
Date received
1984-10-05
Regulation
882.5940
Classification name
Device, Electroconvulsive Therapy
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
RICHARD ABRAMS
Address
910 Sherwood Dr., Unit 17 Lake Bluff IL US 60044 60044

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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