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DIGITAL RADIOGRAPHY SYSTEM, MODEL DFP-8000D

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013608
510(k) Type
Traditional
Applicant
TOSHIBA AMERICA MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2001
Days to Decision
15 days
Submission Type
Summary

DIGITAL RADIOGRAPHY SYSTEM, MODEL DFP-8000D

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013608
510(k) Type
Traditional
Applicant
TOSHIBA AMERICA MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2001
Days to Decision
15 days
Submission Type
Summary