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VERITON CT 300 Series Digital SPECT/CT System (VERITON CT 316/364); VERITON CT 400 Series Digital SPECT/CT System (VERITON CT 416/464)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230600
510(k) Type
Abbreviated
Applicant
Spectrum Dynamics Medical Ltd
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
4/28/2023
Days to Decision
56 days
Submission Type
Summary

VERITON CT 300 Series Digital SPECT/CT System (VERITON CT 316/364); VERITON CT 400 Series Digital SPECT/CT System (VERITON CT 416/464)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230600
510(k) Type
Abbreviated
Applicant
Spectrum Dynamics Medical Ltd
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
4/28/2023
Days to Decision
56 days
Submission Type
Summary