Last synced on 14 November 2025 at 11:06 pm

NEUROSENSOR

Page Type
Cleared 510(K)
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)
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