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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 the device name listed in this FDA 510(k) record. The listed applicant is Qx World, Ltd.. It received FDA 510(k) clearance on 2024-10-11 under 510(k) 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. The listed applicant is Qx World, Ltd.. The 510(k) number is K232779.

When did QUEX ED; QUEX S receive FDA 510(k) clearance?

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

Who is the listed applicant for QUEX ED; QUEX S?

The FDA 510(k) record lists Qx World, Ltd. as the applicant. This does not by itself establish the device manufacturer.

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

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

Related Devices (Code: OMC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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