Last synced on 25 January 2026 at 3:41 am

KODAK CARDIOLOGY DIGITAL ARCHIVE & REVIEW SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960043
510(k) Type
Traditional
Applicant
Jamieson Film Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/1996
Days to Decision
84 days
Submission Type
Statement

KODAK CARDIOLOGY DIGITAL ARCHIVE & REVIEW SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960043
510(k) Type
Traditional
Applicant
Jamieson Film Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/1996
Days to Decision
84 days
Submission Type
Statement