Last synced on 14 November 2025 at 11:06 pm

GAMMAPLAN

Page Type
Cleared 510(K)
510(k) Number
K051022
510(k) Type
Traditional
Applicant
ELEKTA INSTRUMENT AB
Country
Sweden
FDA Decision
Substantially Equivalent
Decision Date
6/1/2005
Days to Decision
40 days
Submission Type
Summary

GAMMAPLAN

Page Type
Cleared 510(K)
510(k) Number
K051022
510(k) Type
Traditional
Applicant
ELEKTA INSTRUMENT AB
Country
Sweden
FDA Decision
Substantially Equivalent
Decision Date
6/1/2005
Days to Decision
40 days
Submission Type
Summary