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MODEL 1320, NEUROLINK II NEUROMONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K970942
510(k) Type
Traditional
Applicant
PHYSIOMETRIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/1997
Days to Decision
80 days
Submission Type
Summary

MODEL 1320, NEUROLINK II NEUROMONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K970942
510(k) Type
Traditional
Applicant
PHYSIOMETRIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/1997
Days to Decision
80 days
Submission Type
Summary