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NEUROSIGN MODEL 100

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923056
510(k) Type
Traditional
Applicant
THE MAGSTIM COMPANY LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
11/24/1992
Days to Decision
153 days
Submission Type
Summary

NEUROSIGN MODEL 100

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923056
510(k) Type
Traditional
Applicant
THE MAGSTIM COMPANY LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
11/24/1992
Days to Decision
153 days
Submission Type
Summary