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DIGITAL RADIOGRAPHY, FLEXDR C30

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082347
510(k) Type
Traditional
Applicant
KONICA MINOLTA TECHNOPRODUCT CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/2008
Days to Decision
95 days
Submission Type
Summary

DIGITAL RADIOGRAPHY, FLEXDR C30

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082347
510(k) Type
Traditional
Applicant
KONICA MINOLTA TECHNOPRODUCT CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/2008
Days to Decision
95 days
Submission Type
Summary