Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in CanadaLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Siemens HealthineersLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Varian Canada, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Sep 26, 1995: HFX350, 30KW, 300MA, 1 OR 3 PHASE RADIOGRAPHIC & FLUOROSCOPIC X-RAY GENERATOR.
| Sep 26, 1995 | HFX350, 30KW, 300MA, 1 OR 3 PHASE RADIOGRAPHIC & FLUOROSCOPIC X-RAY GENERATORK953582 · IZO | 510(k) clearances |
| Dec 28, 1992 | HFG 350, 650, 1050K923455 · KPR | 510(k) clearances |
| Jun 17, 1992 | VJW2919 PNEUMATIC COMPRESSION UPGRADEK920938 · IZH | 510(k) clearances |
| Sep 23, 1991 | VPW2906A1: 480V, 3 PHASE, X-RAY POWER SUPPLYK913234 · IZO | 510(k) clearances |
| Mar 7, 1991 | VPW 2877E6 X-RAY POWER SUPPLYK910820 · IZO | 510(k) clearances |
| Feb 19, 1991 | VPW 2903 A-1 -208V, B2-440V,C3-240V X-RAY SUPPLYK904169 · IZO | 510(k) clearances |
| Feb 13, 1991 | VPW2877E7 X RAY POWER SUPPLYK905855 · IZO | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
