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LEKSELL STEREOTACTIC SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K972324
510(k) Type
Traditional
Applicant
ELEKTA INSTRUMENT AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/1998
Days to Decision
252 days
Submission Type
Summary

LEKSELL STEREOTACTIC SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K972324
510(k) Type
Traditional
Applicant
ELEKTA INSTRUMENT AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/1998
Days to Decision
252 days
Submission Type
Summary