Kubtec Mozart (Xpert42)
K-Number: K183624 · 2019-06-20
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.