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KODAK CARDIOLOGY DIGITAL ARCHIVE & REVIEW SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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