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LEKSELL VIEWSCOPE, LEKSELL SURGISCOPE, LEKSELL FREEHAND

Page Type
Cleared 510(K)
510(k) Number
K973684
510(k) Type
Traditional
Applicant
ELEKTA INSTRUMENT AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1998
Days to Decision
186 days
Submission Type
Summary

LEKSELL VIEWSCOPE, LEKSELL SURGISCOPE, LEKSELL FREEHAND

Page Type
Cleared 510(K)
510(k) Number
K973684
510(k) Type
Traditional
Applicant
ELEKTA INSTRUMENT AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1998
Days to Decision
186 days
Submission Type
Summary