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xPORT 304 (miCOR) System Lens Fragmentation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K200584
510(k) Type
Traditional
Applicant
Carl Zeiss Meditec Cataract Technology Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2020
Days to Decision
147 days
Submission Type
Statement

xPORT 304 (miCOR) System Lens Fragmentation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K200584
510(k) Type
Traditional
Applicant
Carl Zeiss Meditec Cataract Technology Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2020
Days to Decision
147 days
Submission Type
Statement