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LEKSELL SURGIPLAN

Page Type
Cleared 510(K)
510(k) Number
K943468
510(k) Type
Traditional
Applicant
ELEKTA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/1995
Days to Decision
185 days
Submission Type
Summary

LEKSELL SURGIPLAN

Page Type
Cleared 510(K)
510(k) Number
K943468
510(k) Type
Traditional
Applicant
ELEKTA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/1995
Days to Decision
185 days
Submission Type
Summary