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HFX350, 30KW, 300MA, 1 OR 3 PHASE RADIOGRAPHIC & FLUOROSCOPIC X-RAY GENERATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K953582
510(k) Type
Traditional
Applicant
VARIAN CANADA, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
9/26/1995
Days to Decision
56 days
Submission Type
Statement

HFX350, 30KW, 300MA, 1 OR 3 PHASE RADIOGRAPHIC & FLUOROSCOPIC X-RAY GENERATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K953582
510(k) Type
Traditional
Applicant
VARIAN CANADA, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
9/26/1995
Days to Decision
56 days
Submission Type
Statement