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FDA 510(k)

SaintView

K-Number: K223660 · 2023-08-14

ApplicantInviz Corporation
Decision Date2023-08-14
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SaintView is a medical device manufactured by Inviz Corporation. It received FDA 510(k) clearance on 2023-08-14 under approval number K223660. 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 SaintView?

SaintView is a medical device that received FDA 510(k) clearance on 2023-08-14. It is manufactured by Inviz Corporation. The 510(k) number is K223660.

When was SaintView approved by the FDA?

SaintView received FDA 510(k) clearance on 2023-08-14, under approval number K223660.

What company makes SaintView?

SaintView is manufactured by Inviz Corporation.

What is the FDA product code for SaintView?

The FDA product code for SaintView 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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