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KODAK DIRECTVIEW CR 800 SYSTEM, CATALOG# 1268622; KODAK DIRECTVIEW CR 900 SYSTEM, CATALOG# 1170976

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020635
510(k) Type
Special
Applicant
EASTMAN KODAK COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2002
Days to Decision
22 days
Submission Type
Summary

KODAK DIRECTVIEW CR 800 SYSTEM, CATALOG# 1268622; KODAK DIRECTVIEW CR 900 SYSTEM, CATALOG# 1170976

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020635
510(k) Type
Special
Applicant
EASTMAN KODAK COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2002
Days to Decision
22 days
Submission Type
Summary