LHM — System, Thermographic, Liquid Crystal Class I

FDA Device Classification

FDA product code LHM covers "System, Thermographic, Liquid Crystal", a Class I medical device regulated under 21 CFR 884.2982. Submissions are reviewed by the Obstetrics/Gynecology panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
LHM
Device Class
Class I
Regulation Number
884.2982
Submission Type
Review Panel
RA
Medical Specialty
Obstetrics/Gynecology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K872962thermascanBREAST-SCAN(TM)October 20, 1987