Varian Canada, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K953582HFX350, 30KW, 300MA, 1 OR 3 PHASE RADIOGRAPHIC & FLUOROSCOPIC X-RAY GENERATORSeptember 26, 1995
K923455HFG 350, 650, 1050December 28, 1992
K920938VJW2919 PNEUMATIC COMPRESSION UPGRADEJune 17, 1992
K913234VPW2906A1: 480V, 3 PHASE, X-RAY POWER SUPPLYSeptember 23, 1991
K910820VPW 2877E6 X-RAY POWER SUPPLYMarch 7, 1991
K904169VPW 2903 A-1 -208V, B2-440V,C3-240V X-RAY SUPPLYFebruary 19, 1991
K905855VPW2877E7 X RAY POWER SUPPLYFebruary 13, 1991