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FDA 510(k)

Kubtec Mozart Supra

K-Number: K200756 · 2020-06-12

Decision Date2020-06-12
Product CodeMWP
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Kubtec Mozart Supra 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 2020-06-12 under 510(k) number K200756. 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 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

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