FDA.report

Product code LHP

Device name
System, Telethermographic (Sole Diagnostic Screen)
Medical specialty
Obstetrics/Gynecology
Device class
3
Regulation number
884.2980
Review panel
RA
Implant
N
Life sustaining/supporting
N
GMP exempt
N
Third party review
N
Summary malfunction reporting
Eligible
Source
FDA openFDA device classification dataset

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