Last synced on 14 November 2025 at 11:06 pm

MRI PATIENT MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K132359
510(k) Type
Special
Applicant
INVIVO CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/2013
Days to Decision
31 days
Submission Type
Summary

MRI PATIENT MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K132359
510(k) Type
Special
Applicant
INVIVO CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/2013
Days to Decision
31 days
Submission Type
Summary