LQW — Test, Temperature Discrimination Class I

FDA Device Classification

FDA product code LQW covers "Test, Temperature Discrimination", a Class I medical device regulated under 21 CFR 882.1200. Submissions are reviewed by the Neurology panel. At least 3 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
LQW
Device Class
Class I
Regulation Number
882.1200
Submission Type
Review Panel
NE
Medical Specialty
Neurology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K141208prosenexDYNAMIC NEUROSCREENING DEVICEJuly 23, 2014
K922052medocTSA 2001 THERMAL SENSORY ANALYZEROctober 21, 1993
K864345sensortekNTE-2 THERMAL SENSITIVITY TESTERJanuary 29, 1987