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KDR AU-DDR System Advanced U-Arm with Dynamic Digital Radiography, KDR AU System Advanced U-Arm with Static Digital Radiography

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193225
510(k) Type
Traditional
Applicant
Konica Minolta Healthcare Americas, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/15/2020
Days to Decision
54 days
Submission Type
Summary

KDR AU-DDR System Advanced U-Arm with Dynamic Digital Radiography, KDR AU System Advanced U-Arm with Static Digital Radiography

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193225
510(k) Type
Traditional
Applicant
Konica Minolta Healthcare Americas, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/15/2020
Days to Decision
54 days
Submission Type
Summary