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HYBRID SURGICAL DEVICE MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K935258
510(k) Type
Traditional
Applicant
LCA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/1994
Days to Decision
73 days
Submission Type
Statement

HYBRID SURGICAL DEVICE MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K935258
510(k) Type
Traditional
Applicant
LCA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/1994
Days to Decision
73 days
Submission Type
Statement