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RAD II SIMULATOR, RAD II KV IMAGER, DUAL RAD II KV IMAGER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101038
510(k) Type
Traditional
Applicant
ACCELETRONICS DIGITAL IMAGING, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/2010
Days to Decision
125 days
Submission Type
Summary

RAD II SIMULATOR, RAD II KV IMAGER, DUAL RAD II KV IMAGER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101038
510(k) Type
Traditional
Applicant
ACCELETRONICS DIGITAL IMAGING, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/2010
Days to Decision
125 days
Submission Type
Summary