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FDA 510(k)

QUEX ED; QUEX S

K-Number: K232779 · 2024-10-11

ApplicantQx World, Ltd.
Decision Date2024-10-11
Product CodeOMC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

QUEX ED; QUEX S is a medical device manufactured by Qx World, Ltd.. It received FDA 510(k) clearance on 2024-10-11 under approval number K232779. The device is classified under product code OMC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUEX ED; QUEX S?

QUEX ED; QUEX S is a medical device that received FDA 510(k) clearance on 2024-10-11. It is manufactured by Qx World, Ltd.. The 510(k) number is K232779.

When was QUEX ED; QUEX S approved by the FDA?

QUEX ED; QUEX S received FDA 510(k) clearance on 2024-10-11, under approval number K232779.

What company makes QUEX ED; QUEX S?

QUEX ED; QUEX S is manufactured by Qx World, Ltd..

What is the FDA product code for QUEX ED; QUEX S?

The FDA product code for QUEX ED; QUEX S is OMC.

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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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