Last synced on 15 September 2023 at 11:04 pm

NEUROSOFT'S SOURCE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011241
510(k) Type
Traditional
Applicant
NEUROSOFT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2001
Days to Decision
149 days
Submission Type
Summary

NEUROSOFT'S SOURCE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011241
510(k) Type
Traditional
Applicant
NEUROSOFT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2001
Days to Decision
149 days
Submission Type
Summary