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FEMTO LDV(TM) Z-GENERATION FEMTOSECOND SURGICAL LASER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131207
510(k) Type
Traditional
Applicant
SURGICAL INSTRUMENT ENGINEERING AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/2013
Days to Decision
163 days
Submission Type
Summary

FEMTO LDV(TM) Z-GENERATION FEMTOSECOND SURGICAL LASER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131207
510(k) Type
Traditional
Applicant
SURGICAL INSTRUMENT ENGINEERING AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/2013
Days to Decision
163 days
Submission Type
Summary