Last synced on 20 December 2024 at 11:05 pm

3D ANGIOGRAPHIC IMAGING SYSTEM, MODEL XIDF-100A

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002424
510(k) Type
Traditional
Applicant
TOSHIBA AMERICA MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/2000
Days to Decision
80 days
Submission Type
Summary

3D ANGIOGRAPHIC IMAGING SYSTEM, MODEL XIDF-100A

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002424
510(k) Type
Traditional
Applicant
TOSHIBA AMERICA MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/2000
Days to Decision
80 days
Submission Type
Summary