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MAMMOGRAPHY PRO, MODEL 13017, DIAGNOSTIC PRO W/ MAMMOGRAPHY OPTION, MODEL 13205

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993598
510(k) Type
Traditional
Applicant
VIDAR SYSTEMS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/2000
Days to Decision
87 days
Submission Type
Summary

MAMMOGRAPHY PRO, MODEL 13017, DIAGNOSTIC PRO W/ MAMMOGRAPHY OPTION, MODEL 13205

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993598
510(k) Type
Traditional
Applicant
VIDAR SYSTEMS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/2000
Days to Decision
87 days
Submission Type
Summary