ClearanceBrief
Company ยท CA

Varian Canada, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1991 to 1995. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
IZOGenerator, High-Voltage, X-Ray, Diagnostic5
IZHSystem, X-Ray, Mammographic1
KPRSystem, X-Ray, Stationary1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 26, 1995K953582HFX350, 30KW, 300MA, 1 OR 3 PHASE RADIOGRAPHIC & FLUOROSCOPIC X-RAY GENERATOR
Varian Canada, Inc., CA
IZO
Dec 28, 1992K923455HFG 350, 650, 1050
Varian Canada, Inc., CA
KPR
Jun 17, 1992K920938VJW2919 PNEUMATIC COMPRESSION UPGRADE
Varian Canada, Inc., CA
IZH
Sep 23, 1991K913234VPW2906A1: 480V, 3 PHASE, X-RAY POWER SUPPLY
Varian Canada, Inc., CA
IZO
Mar 7, 1991K910820VPW 2877E6 X-RAY POWER SUPPLY
Varian Canada, Inc., CA
IZO
Feb 19, 1991K904169VPW 2903 A-1 -208V, B2-440V,C3-240V X-RAY SUPPLY
Varian Canada, Inc., CA
IZO
Feb 13, 1991K905855VPW2877E7 X RAY POWER SUPPLY
Varian Canada, Inc., CA
IZO

Latest recalls

DateFirm and productCodeLinked 510(k)
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