Last synced on 14 November 2025 at 11:06 pm

Philips MR Patient Care Portal

Page Type
Cleared 510(K)
510(k) Number
K212227
510(k) Type
Traditional
Applicant
Invivo Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/2021
Days to Decision
76 days
Submission Type
Summary

Philips MR Patient Care Portal

Page Type
Cleared 510(K)
510(k) Number
K212227
510(k) Type
Traditional
Applicant
Invivo Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/2021
Days to Decision
76 days
Submission Type
Summary