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510(k) K922052

Device
TSA 2001 THERMAL SENSORY ANALYZER
Applicant
MEDOC CORP.
510(k) number
K922052
Product code
LQW  
Decision
Substantially Equivalent (SESE)
Decision date
1993-10-21
Date received
1992-05-04
Regulation
882.1200
Classification name
Test, Temperature Discrimination
Medical specialty
Neurology
Review panel
Neurology
Device class
1
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
EMANUEL A ROSEN
Address
P.O. Box 1309 88112 Eilat, Israel Eilat IL

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code LQW  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K141208DYNAMIC NEUROSCREENING DEVICEProsenex2014-07-23
K864345NTE-2 THERMAL SENSITIVITY TESTERSensortek, Inc.1987-01-29

Legacy Summary#

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FDA Review#

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