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DG 200/300 DIGITAL ANGIOGRAPHIC SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852353
510(k) Type
Traditional
Applicant
THOMSON-CGR MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/1985
Days to Decision
65 days

DG 200/300 DIGITAL ANGIOGRAPHIC SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852353
510(k) Type
Traditional
Applicant
THOMSON-CGR MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/1985
Days to Decision
65 days