# Varian Canada, Inc.

- Location (FDA's records): Canada L7g 2j4, CA
- FDA decisions: 7 (1991–1995): 7 510(k) clearances
- Product codes: IZO (5), IZH (1), KPR (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K953582: HFX350, 30KW, 300MA, 1 or 3 Phase Radiographic & Fluoroscopic X-Ray Generator (Sep 26, 1995)
- K923455: HFG 350, 650, 1050 (Dec 28, 1992)
- K920938: VJW2919 Pneumatic Compression Upgrade (Jun 17, 1992)
- K913234: VPW2906A1: 480V, 3 Phase, X-Ray Power Supply (Sep 23, 1991)
- K910820: VPW 2877E6 X-Ray Power Supply (Mar 7, 1991)
- K904169: VPW 2903 a-1 -208V, B2-440V,C3-240V X-Ray Supply (Feb 19, 1991)
- K905855: VPW2877E7 X Ray Power Supply (Feb 13, 1991)

Source page: https://510kreport.com/company/varian-canada