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DRAD3000E/RADREX-I

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082494
510(k) Type
Traditional
Applicant
Toshiba America Medical Systems, In.C
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2008
Days to Decision
14 days
Submission Type
Summary

DRAD3000E/RADREX-I

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082494
510(k) Type
Traditional
Applicant
Toshiba America Medical Systems, In.C
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2008
Days to Decision
14 days
Submission Type
Summary