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FDA 510(k)

Kubtec Mozart (Xpert42)

K-Number: K183624 · 2019-06-20

Decision Date2019-06-20
Product CodeMWP
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Kubtec Mozart (Xpert42) is the device name listed in this FDA 510(k) record. The listed applicant is Kub Technologies, Inc.. It received FDA 510(k) clearance on 2019-06-20 under 510(k) number K183624. The device is classified under product code MWP. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Kubtec Mozart (Xpert42)?

Kubtec Mozart (Xpert42) is a medical device that received FDA 510(k) clearance on 2019-06-20. The listed applicant is Kub Technologies, Inc.. The 510(k) number is K183624.

When did Kubtec Mozart (Xpert42) receive FDA 510(k) clearance?

Kubtec Mozart (Xpert42) received FDA 510(k) clearance on 2019-06-20, under 510(k) number K183624.

Who is the listed applicant for Kubtec Mozart (Xpert42)?

The FDA 510(k) record lists Kub Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Kubtec Mozart (Xpert42)?

The FDA product code for Kubtec Mozart (Xpert42) is MWP.

Other records listing Kub Technologies, Inc. as applicant

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.

Related Devices (Code: MWP)

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.

Official Source

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