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NT 2000 LESIONING GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K111576
510(k) Type
Traditional
Applicant
NEUROTHERM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/20/2011
Days to Decision
106 days
Submission Type
Summary

NT 2000 LESIONING GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K111576
510(k) Type
Traditional
Applicant
NEUROTHERM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/20/2011
Days to Decision
106 days
Submission Type
Summary