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NEUROVISION NERVE LOCATOR MONITOR

Page Type
Cleared 510(K)
510(k) Number
K110140
510(k) Type
Traditional
Applicant
NEUROVISION MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/2011
Days to Decision
255 days
Submission Type
Summary

NEUROVISION NERVE LOCATOR MONITOR

Page Type
Cleared 510(K)
510(k) Number
K110140
510(k) Type
Traditional
Applicant
NEUROVISION MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/2011
Days to Decision
255 days
Submission Type
Summary