Canon Inc. -Medical Equipment Group is one of 79 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Canon Inc. -Medical Equipment Group - FDA 510(k) Cleared Devices
Recent clearances: Ophthalmic Software Platform RX
11
Total
11
Cleared
0
Denied
Canon Inc. -Medical Equipment Group has 11 FDA 510(k) cleared medical devices. Based in Tachikawa-Shi, Tokyo, JP.
Historical record: 11 cleared submissions from 2010 to 2018. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Canon Inc. -Medical Equipment Group Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ora, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Canon Inc. -Medical Equipment Group
11 devices
Cleared
Feb 23, 2018
Ophthalmic Software Platform RX
Ophthalmic
84d
Cleared
Jan 27, 2017
CSX-30 Flat Panel Detector
Radiology
102d
Cleared
Mar 19, 2013
DIGITAL RETINAL CAMERA
Ophthalmic
158d
Cleared
Jul 26, 2012
MOBILE C-ARM
Radiology
86d
Cleared
Apr 23, 2012
FLAT PANEL DETECTOR
Radiology
300d
Cleared
Sep 20, 2011
FULL AUTO TONOMETER MODEL TX-20
Ophthalmic
92d
Cleared
Sep 02, 2011
DIGITAL RADIOGRAPHY
Radiology
79d
Cleared
Sep 02, 2011
DIGITAL RADIOGRAPHY
Radiology
22d
Cleared
Mar 29, 2011
DIGITAL RADIOGRAPHY
Radiology
112d
Cleared
Oct 29, 2010
DIGITAL RETINAL CAMERA
Ophthalmic
105d
Cleared
Aug 17, 2010
DIGITAL RADIOGRAPHY
Radiology
32d