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FDA 510(k)

MIDASVu

K-Number: K243020 · 2024-12-02

ApplicantIntravu, Inc.
Decision Date2024-12-02
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MIDASVu is a medical device manufactured by Intravu, Inc.. It received FDA 510(k) clearance on 2024-12-02 under approval number K243020. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIDASVu?

MIDASVu is a medical device that received FDA 510(k) clearance on 2024-12-02. It is manufactured by Intravu, Inc.. The 510(k) number is K243020.

When was MIDASVu approved by the FDA?

MIDASVu received FDA 510(k) clearance on 2024-12-02, under approval number K243020.

What company makes MIDASVu?

MIDASVu is manufactured by Intravu, Inc..

What is the FDA product code for MIDASVu?

The FDA product code for MIDASVu is HRX.

Other Devices by Intravu, Inc.

K181982MIDAScope and Introducer Kit, and MIDASystem

Related Devices (Code: HRX)

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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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