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EYETECH-VISION SCREENING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K803256
510(k) Type
Traditional
Applicant
EYEDEX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1981
Days to Decision
71 days

EYETECH-VISION SCREENING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K803256
510(k) Type
Traditional
Applicant
EYEDEX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1981
Days to Decision
71 days