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DISCOVERY MODEL CT590 RT AND OPTIMA MODEL CT580 CT SYSTEMS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093581
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2011
Days to Decision
517 days
Submission Type
Summary

DISCOVERY MODEL CT590 RT AND OPTIMA MODEL CT580 CT SYSTEMS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093581
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2011
Days to Decision
517 days
Submission Type
Summary