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MICOR 700 with Auto I/A

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243395
510(k) Type
Traditional
Applicant
Carl Zeiss Meditec Cataract Technology, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2025
Days to Decision
281 days
Submission Type
Statement

MICOR 700 with Auto I/A

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243395
510(k) Type
Traditional
Applicant
Carl Zeiss Meditec Cataract Technology, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2025
Days to Decision
281 days
Submission Type
Statement