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3160 MRI PATIENT MONITORING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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