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NEUROVIEW COAXIAL BIPOLAR ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K955351
510(k) Type
Traditional
Applicant
NEURO NAVIGATIONAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/29/1996
Days to Decision
100 days
Submission Type
Statement

NEUROVIEW COAXIAL BIPOLAR ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K955351
510(k) Type
Traditional
Applicant
NEURO NAVIGATIONAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/29/1996
Days to Decision
100 days
Submission Type
Statement