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KODAK EKTACHEM 500/750 SERIES ANALYZER, SOFT V1.0

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890927
510(k) Type
Traditional
Applicant
EASTMAN KODAK COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/1989
Days to Decision
32 days

KODAK EKTACHEM 500/750 SERIES ANALYZER, SOFT V1.0

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890927
510(k) Type
Traditional
Applicant
EASTMAN KODAK COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/1989
Days to Decision
32 days