Varian Canada, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Varian Canada, Inc. has 7 FDA 510(k) cleared medical devices. Based in Canada L7g 2j4, CA.
Historical record: 7 cleared submissions from 1991 to 1995. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Varian Canada, Inc. Filter by specialty or product code using the sidebar.
7 devices
Cleared
Sep 26, 1995
HFX350, 30KW, 300MA, 1 OR 3 PHASE RADIOGRAPHIC & FLUOROSCOPIC X-RAY GENERATOR
Radiology
56d
Cleared
Dec 28, 1992
HFG 350, 650, 1050
Radiology
167d
Cleared
Jun 17, 1992
VJW2919 PNEUMATIC COMPRESSION UPGRADE
Radiology
111d
Cleared
Sep 23, 1991
VPW2906A1: 480V, 3 PHASE, X-RAY POWER SUPPLY
Radiology
63d
Cleared
Mar 07, 1991
VPW 2877E6 X-RAY POWER SUPPLY
Radiology
10d
Cleared
Feb 19, 1991
VPW 2903 A-1 -208V, B2-440V,C3-240V X-RAY SUPPLY
Radiology
161d
Cleared
Feb 13, 1991
VPW2877E7 X RAY POWER SUPPLY
Radiology
54d