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FDA 510(k)

XPERT 40 SPECIMEN RADIOGRAPHY SYSTEM

K-Number: K071233 · 2007-06-20

ApplicantKub Technologies, Inc.
Decision Date2007-06-20
Product CodeMWP
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

XPERT 40 SPECIMEN RADIOGRAPHY SYSTEM 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 2007-06-20 under 510(k) number K071233. 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 XPERT 40 SPECIMEN RADIOGRAPHY SYSTEM?

XPERT 40 SPECIMEN RADIOGRAPHY SYSTEM is a medical device that received FDA 510(k) clearance on 2007-06-20. The listed applicant is Kub Technologies, Inc.. The 510(k) number is K071233.

When did XPERT 40 SPECIMEN RADIOGRAPHY SYSTEM receive FDA 510(k) clearance?

XPERT 40 SPECIMEN RADIOGRAPHY SYSTEM received FDA 510(k) clearance on 2007-06-20, under 510(k) number K071233.

Who is the listed applicant for XPERT 40 SPECIMEN RADIOGRAPHY SYSTEM?

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 XPERT 40 SPECIMEN RADIOGRAPHY SYSTEM?

The FDA product code for XPERT 40 SPECIMEN RADIOGRAPHY SYSTEM is MWP.

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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.

K210955Kubtec Mozart Supra (XPERT 84) Radiography SystemK210956Kubtec Mozart (XPERT42)K210957Kubec Xpert 80 Radiography SystemK200756Kubtec Mozart SupraK183624Kubtec Mozart (Xpert42)K103348DIGIVIEW 250

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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.

K230140TrueView Core 100Pro-US Core Specimen Radiography System (TrueView Core 100Pro-US)Compai Healthcare (Suzhou) Co.,LtdK230136TrueView 200 Pro-US Specimen Radiography System (TrueView 200 Pro-US)Compai Healthcare (Suzhou) Co.,LtdK213691Solas ORCirdan Imaging, Ltd.K210955Kubtec Mozart Supra (XPERT 84) Radiography SystemKub Technologies, Inc.K210956Kubtec Mozart (XPERT42)Kub Technologies, Inc.K210957Kubec Xpert 80 Radiography SystemKub Technologies, Inc.

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.

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