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FDR ACSELERATE SYSTEM, DR-ID 200 FLAT PANEL DETECTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093427
510(k) Type
Abbreviated
Applicant
FUJIFILM MEDICAL SYSTEM U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/2010
Days to Decision
79 days
Submission Type
Statement

FDR ACSELERATE SYSTEM, DR-ID 200 FLAT PANEL DETECTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093427
510(k) Type
Abbreviated
Applicant
FUJIFILM MEDICAL SYSTEM U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/2010
Days to Decision
79 days
Submission Type
Statement