QUBYX receives FDA clearance for OptikView Display in bundle with PerfectLum DICOM calibration software

Wilmington, DE., April, 15,2020 - QUBYX is excited to announce, that it again received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for a display bundle with QUBYX PerfectLum DICOM calibration software. 

“We are extremely happy with FDA's decision to approve the OptikView & PerfectLum Bundle.” - says Marc Leppla, Director and CTO of QUBYX. “Our long-term development has become very rewarding this year.”

Optikview Gup2103cmi overview
The OptikView Gup2103cmi is a 21” 3MP monitor which is designed specifically for the demanding medical imaging environment. The FDA 510(k) number isK191705
Previously PerfectLum did receive FDA clearance with the following displays:
Dell Ultrasharp U3011 W/Qubyx Perfectlum BundleK111385
Dell U3014 With Qubyx Perfectlum BundleK131601
Diva Zsp5812cmi With Qubyx Perfectlum BundleK152847
Dell Up3216q With Qubyx Perfectlum BundleK162196
Dell Up3017 With Qubyx Perfectlum BundleK171229
Diva Zsp2105cmi With Qubyx Perfectlum BundleK160328

PerfectLum software overview
QUBYX PerfectLum is a calibration and quality control application that significantly enhances the performance of any display in accordance with medical imaging requirements, including NEMA DICOM part 14 GSDF. The software also performs acceptance and constancy tests to verify that the display conforms to such regulations as AAPM TG18, new DIN 6868-157, JESRA X-0093, IEC 62563-1, ACR, NY State PDM and NY City PDM Guidelines.

According to the recently issued FDA 510(k) clearance, the bundle of Optikview Gup2103cmi monitor & QUBYX PerfectLum is intended to be used for displaying and viewing medical images, for review and analysis by trained medical practitioners.

About QUBYX
QUBYX, a software manufacturer providing the new dimension of image quality in the medical imaging industry and display calibration field since 2002. For more information about the company visit www.qubyx.co

Accounting for VAT registration on a cash basis are applicable only for those whose annual business gross income does not exceed a public authority, local authority or a non-profit body. There are 4 categories for lodgment of VAT registration returns under the respective taxable periods. They are monthly returns; 3-month returns; 12 month returns for produce suppliers primarily engaged and 12 month returns for small and medium businesses with an annual gross turnover. A business person may request in writing to the CEO if the annual gross sales do not exceeded the required amount. However, we would need to notify FRCA to be changed to a monthly basis once the annual gross sales exceed this amount.

Will Muthirai give advice on whether to register for VAT and assist in the completion and what happens if a business person wants to deregister from VAT?

Definitely we will assist and advise taxpayers on any issues from VAT registration and all its procedure. We facilitate to improve voluntary compliance for taxpayers. Our customer enquiry centers are there to assist all taxpayers. Our customer enquiry centers are experienced staff in all tax types. We’ll not fill in the VAT returns for you but will assist you in completing it. To degister from VAT a registered person will need to write a request for deregistration. A deregistration audit will be conducted to determine whether the person is qualified for deregistration. For deregistration all the business assets and stock will be valued. Once the audit is completed and the tax arrears is cleared, the person will be notified in deregistration. During this process, you will still be required to lodge your VAT returns until you receive a confirmation on deregistration.

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