Last synced on 14 November 2025 at 11:06 pm

xPORT Lens Fragmentation System

Page Type
Cleared 510(K)
510(k) Number
K191024
510(k) Type
Traditional
Applicant
Carl Zeiss Meditec Cataract Technology Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2019
Days to Decision
117 days
Submission Type
Statement

xPORT Lens Fragmentation System

Page Type
Cleared 510(K)
510(k) Number
K191024
510(k) Type
Traditional
Applicant
Carl Zeiss Meditec Cataract Technology Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2019
Days to Decision
117 days
Submission Type
Statement