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FDA 510(k)

Centricity Universal Viewer

K-Number: K182419 · 2018-12-14

ApplicantGE Healthcare
Decision Date2018-12-14
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Centricity Universal Viewer is a medical device manufactured by GE Healthcare. It received FDA 510(k) clearance on 2018-12-14 under approval number K182419. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Centricity Universal Viewer?

Centricity Universal Viewer is a medical device that received FDA 510(k) clearance on 2018-12-14. It is manufactured by GE Healthcare. The 510(k) number is K182419.

When was Centricity Universal Viewer approved by the FDA?

Centricity Universal Viewer received FDA 510(k) clearance on 2018-12-14, under approval number K182419.

What company makes Centricity Universal Viewer?

Centricity Universal Viewer is manufactured by GE Healthcare.

What is the FDA product code for Centricity Universal Viewer?

The FDA product code for Centricity Universal Viewer is LLZ.

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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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