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FEMTO LDV

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112154
510(k) Type
Traditional
Applicant
Sie Ag,Surgical Instument Engineering
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/2012
Days to Decision
233 days
Submission Type
Statement

FEMTO LDV

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112154
510(k) Type
Traditional
Applicant
Sie Ag,Surgical Instument Engineering
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/2012
Days to Decision
233 days
Submission Type
Statement