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SYNERAD OMNI, DIGITAL X-RAY SYSTEM, MODEL AN6250

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043025
510(k) Type
Abbreviated
Applicant
Analogic Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2004
Days to Decision
16 days
Submission Type
Summary

SYNERAD OMNI, DIGITAL X-RAY SYSTEM, MODEL AN6250

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043025
510(k) Type
Abbreviated
Applicant
Analogic Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2004
Days to Decision
16 days
Submission Type
Summary