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ELEKTA STEREOTACTIC GUIDE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991636
510(k) Type
Traditional
Applicant
Elekta Instrument AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/1999
Days to Decision
69 days
Submission Type
Summary

ELEKTA STEREOTACTIC GUIDE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991636
510(k) Type
Traditional
Applicant
Elekta Instrument AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/1999
Days to Decision
69 days
Submission Type
Summary