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LEKSELL NEURO GENERATOR AND ACCESSORIES

Page Type
Cleared 510(K)
510(k) Number
K941823
510(k) Type
Traditional
Applicant
ELEKTA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/1996
Days to Decision
709 days
Submission Type
Statement

LEKSELL NEURO GENERATOR AND ACCESSORIES

Page Type
Cleared 510(K)
510(k) Number
K941823
510(k) Type
Traditional
Applicant
ELEKTA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/1996
Days to Decision
709 days
Submission Type
Statement