Last synced on 20 December 2024 at 11:05 pm

NEUROSCREEN SOFTWARE FOR USE WITH THE NEUROSIGN 100 NERVE MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951641
510(k) Type
Traditional
Applicant
THE MAGSTIM COMPANY LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
5/9/1995
Days to Decision
49 days
Submission Type
Summary

NEUROSCREEN SOFTWARE FOR USE WITH THE NEUROSIGN 100 NERVE MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951641
510(k) Type
Traditional
Applicant
THE MAGSTIM COMPANY LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
5/9/1995
Days to Decision
49 days
Submission Type
Summary