Kubtec Mozart Supra
K-Number: K200756 · 2020-06-12
Device Summary
Frequently Asked Questions
What is the Kubtec Mozart Supra?
Kubtec Mozart Supra is a medical device that received FDA 510(k) clearance on 2020-06-12. The listed applicant is Kub Technologies, Inc.. The 510(k) number is K200756.
When did Kubtec Mozart Supra receive FDA 510(k) clearance?
Kubtec Mozart Supra received FDA 510(k) clearance on 2020-06-12, under 510(k) number K200756.
Who is the listed applicant for Kubtec Mozart Supra?
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 Supra?
The FDA product code for Kubtec Mozart Supra 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.