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MRI COMPATIBLE PATIENT MONITORING SYSTEM, MODEL 865214

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090785
510(k) Type
Special
Applicant
INVIVO CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/2009
Days to Decision
267 days
Submission Type
Summary

MRI COMPATIBLE PATIENT MONITORING SYSTEM, MODEL 865214

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090785
510(k) Type
Special
Applicant
INVIVO CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/2009
Days to Decision
267 days
Submission Type
Summary