Last synced on 25 January 2026 at 3:41 am

CONTROL, X-RAY DIAGNOSTIC, GENERATOR, HIGH VOLTAGE, ASSEMBLY, TUBE HOUSING DIAGNOSTIC, BEAM LIMITING DEVICE, MANUAL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973833
510(k) Type
Traditional
Applicant
Dynarad Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/1997
Days to Decision
84 days
Submission Type
Statement

CONTROL, X-RAY DIAGNOSTIC, GENERATOR, HIGH VOLTAGE, ASSEMBLY, TUBE HOUSING DIAGNOSTIC, BEAM LIMITING DEVICE, MANUAL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973833
510(k) Type
Traditional
Applicant
Dynarad Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/1997
Days to Decision
84 days
Submission Type
Statement