Viz HDS, Viz Volume Plus, Viz ICH+
K-Number: K232363 · 2024-02-05
ApplicantViz. Ai, Inc.
Decision Date2024-02-05
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Viz HDS, Viz Volume Plus, Viz ICH+ is a medical device manufactured by Viz. Ai, Inc.. It received FDA 510(k) clearance on 2024-02-05 under approval number K232363. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Viz HDS, Viz Volume Plus, Viz ICH+?
Viz HDS, Viz Volume Plus, Viz ICH+ is a medical device that received FDA 510(k) clearance on 2024-02-05. It is manufactured by Viz. Ai, Inc.. The 510(k) number is K232363.
When was Viz HDS, Viz Volume Plus, Viz ICH+ approved by the FDA?
Viz HDS, Viz Volume Plus, Viz ICH+ received FDA 510(k) clearance on 2024-02-05, under approval number K232363.
What company makes Viz HDS, Viz Volume Plus, Viz ICH+?
Viz HDS, Viz Volume Plus, Viz ICH+ is manufactured by Viz. Ai, Inc..
What is the FDA product code for Viz HDS, Viz Volume Plus, Viz ICH+?
The FDA product code for Viz HDS, Viz Volume Plus, Viz ICH+ is QIH.
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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.