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MRI COMPATIBLE PATIENT MONITORING SYSTEM, MODEL 3160

Page Type
Cleared 510(K)
510(k) Number
K050399
510(k) Type
Traditional
Applicant
INVIVO RESEARCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/26/2005
Days to Decision
191 days
Submission Type
Summary

MRI COMPATIBLE PATIENT MONITORING SYSTEM, MODEL 3160

Page Type
Cleared 510(K)
510(k) Number
K050399
510(k) Type
Traditional
Applicant
INVIVO RESEARCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/26/2005
Days to Decision
191 days
Submission Type
Summary