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Canon Inc. -Medical Equipment Group

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K173689Ophthalmic Software Platform RXFebruary 23, 2018
K123208DIGITAL RETINAL CAMERAMarch 19, 2013
K121303MOBILE C-ARMJuly 26, 2012
K111824FLAT PANEL DETECTORApril 23, 2012
K111710FULL AUTO TONOMETER MODEL TX-20September 20, 2011
K112309DIGITAL RADIOGRAPHYSeptember 2, 2011
K111682DIGITAL RADIOGRAPHYSeptember 2, 2011
K103591DIGITAL RADIOGRAPHYMarch 29, 2011
K102013DIGITAL RETINAL CAMERAOctober 29, 2010
K102012DIGITAL RADIOGRAPHYAugust 17, 2010