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3160 MRI PATIENT MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K053462
510(k) Type
Special
Applicant
INVIVO CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/2006
Days to Decision
36 days
Submission Type
Summary

3160 MRI PATIENT MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K053462
510(k) Type
Special
Applicant
INVIVO CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/2006
Days to Decision
36 days
Submission Type
Summary