Kubtec Mozart Supra (XPERT 84) Radiography System— 510(k) K210955

Name: FDA 510(k) clearance K210955
Creator: U.S. Food and Drug Administration
Published: 2021-09-20

Substantially Equivalent

Kub Technologies, Inc.

FDA 510(k) clearance K210955 for Kubtec Mozart Supra (XPERT 84) Radiography System, Substantially Equivalent on 2021-09-20. Applicant: Kub Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Kub Technologies, Inc.
Product code: Code MWP
Device class: Class 2
Regulation: 21 CFR 892.1680
Advisory panel: Radiology
Date received: 2021-03-30
Decision date: 2021-09-20
Decision: Substantially Equivalent
Clearance type: Special
Location: Stratford, CT, US

Download summary PDF View on FDA.gov ↗

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K210957 — Kubec Xpert 80 Radiography System2021-08-31

More clearances from Kub Technologies, Inc.

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K200756 — Kubtec Mozart Supra2020-06-12
K183624 — Kubtec Mozart (Xpert42)2019-06-20
K151221 — Kubtec DIGIVIEW 3952015-06-23
K141539 — KUBTEC X2502014-10-29
K103348 — DIGIVIEW 2502011-10-20

Data sourced from openFDA. This site is unofficial and independent of the FDA.