510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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LHMClass I

System, Thermographic, Liquid Crystal

21 CFR 884.2982 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

LHM is the FDA product code for System, Thermographic, Liquid Crystal, a class I device type, regulated under 21 CFR 884.2982. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
LHM
Device name
System, Thermographic, Liquid Crystal
Regulation
21 CFR 884.2982
Device class
Class I
Review panel
Obstetrics/Gynecology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code LHM

By decision year
1 clearance under product code LHM with a decision year between 1987 and 1987, 1987 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LHM by decision year
YearClearances
19871

Applicants with the most clearances

Product code LHM
Applicants holding the most 510(k) clearances under product code LHM
ApplicantClearances
Thermascan, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code LHM.