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RESCAN 700, CALLISTO eye

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180229
510(k) Type
Traditional
Applicant
Carl Zeiss Meditec AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
1/11/2019
Days to Decision
350 days
Submission Type
Summary

RESCAN 700, CALLISTO eye

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180229
510(k) Type
Traditional
Applicant
Carl Zeiss Meditec AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
1/11/2019
Days to Decision
350 days
Submission Type
Summary