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NEURODRIVE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051830
510(k) Type
Traditional
Applicant
ALPHA OMEGA LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
9/16/2005
Days to Decision
72 days
Submission Type
Statement

NEURODRIVE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051830
510(k) Type
Traditional
Applicant
ALPHA OMEGA LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
9/16/2005
Days to Decision
72 days
Submission Type
Statement