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NEUROMED MODEL 1992 LS LAMITRODE LEAD

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