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Infrascan, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K241389
Infrascanner Model 2500 (Model 2500)
December 12, 2024
K211617
Infrascanner
February 9, 2022
K200203
Infrascanner
July 10, 2020
K120949
INFRASCANNER
January 11, 2013
DEN100002
INFRASCANNER, MODEL 1000
December 13, 2011