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xPORT 304 (miCOR) System Lens Fragmentation System

Page Type
Cleared 510(K)
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)
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