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FEMTO LDV

Page Type
Cleared 510(K)
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)
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