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FDA 510(k)

ViewPoint 6

K-Number: K241300 · 2024-07-02

ApplicantGe Healthcare GmbH
Decision Date2024-07-02
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ViewPoint 6 is a medical device manufactured by Ge Healthcare GmbH. It received FDA 510(k) clearance on 2024-07-02 under approval number K241300. 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 ViewPoint 6?

ViewPoint 6 is a medical device that received FDA 510(k) clearance on 2024-07-02. It is manufactured by Ge Healthcare GmbH. The 510(k) number is K241300.

When was ViewPoint 6 approved by the FDA?

ViewPoint 6 received FDA 510(k) clearance on 2024-07-02, under approval number K241300.

What company makes ViewPoint 6?

ViewPoint 6 is manufactured by Ge Healthcare GmbH.

What is the FDA product code for ViewPoint 6?

The FDA product code for ViewPoint 6 is LLZ.

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Official Source

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

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