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NEUROMED MODEL 1992 LS LAMITRODE LEAD

Page Type
Cleared 510(K)
510(k) Number
K905255
510(k) Type
Traditional
Applicant
NEUROMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/1991
Days to Decision
65 days

NEUROMED MODEL 1992 LS LAMITRODE LEAD

Page Type
Cleared 510(K)
510(k) Number
K905255
510(k) Type
Traditional
Applicant
NEUROMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/1991
Days to Decision
65 days