Last synced on 17 May 2024 at 11:06 pm

LEKSELL VIEWSCOPE, LEKSELL SURGISCOPE, LEKSELL FREEHAND

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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