Last synced on 20 December 2024 at 11:05 pm

NEUROSENSOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013930
510(k) Type
Traditional
Applicant
NOVUS MONITORING LTD
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
2/20/2002
Days to Decision
84 days
Submission Type
Summary

NEUROSENSOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013930
510(k) Type
Traditional
Applicant
NOVUS MONITORING LTD
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
2/20/2002
Days to Decision
84 days
Submission Type
Summary