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xPORT S Lens Fragmentation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K200207
510(k) Type
Traditional
Applicant
Carl Zeiss Meditec Cataract Technology Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2020
Days to Decision
261 days
Submission Type
Statement

xPORT S Lens Fragmentation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K200207
510(k) Type
Traditional
Applicant
Carl Zeiss Meditec Cataract Technology Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2020
Days to Decision
261 days
Submission Type
Statement