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FDA 510(k)

Philips MR Patient Care Portal

K-Number: K212227 · 2021-09-30

ApplicantInvivo Corporation
Decision Date2021-09-30
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Philips MR Patient Care Portal is a medical device manufactured by Invivo Corporation. It received FDA 510(k) clearance on 2021-09-30 under approval number K212227. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Philips MR Patient Care Portal?

Philips MR Patient Care Portal is a medical device that received FDA 510(k) clearance on 2021-09-30. It is manufactured by Invivo Corporation. The 510(k) number is K212227.

When was Philips MR Patient Care Portal approved by the FDA?

Philips MR Patient Care Portal received FDA 510(k) clearance on 2021-09-30, under approval number K212227.

What company makes Philips MR Patient Care Portal?

Philips MR Patient Care Portal is manufactured by Invivo Corporation.

What is the FDA product code for Philips MR Patient Care Portal?

The FDA product code for Philips MR Patient Care Portal is MWI.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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