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FEMTO LDV Z8 Femtosecond Surgical Laser

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213559
510(k) Type
Traditional
Applicant
SIE AG, Surgical Instrument Engineering
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
4/21/2022
Days to Decision
168 days
Submission Type
Summary

FEMTO LDV Z8 Femtosecond Surgical Laser

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213559
510(k) Type
Traditional
Applicant
SIE AG, Surgical Instrument Engineering
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
4/21/2022
Days to Decision
168 days
Submission Type
Summary