FDA 510(k)

Mobius3D

K-Number: K192424 · 2019-10-03

Decision Date2019-10-03

Product CodeIYE

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Mobius3D is a medical device manufactured by Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2019-10-03 under approval number K192424. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Mobius3D?

Mobius3D is a medical device that received FDA 510(k) clearance on 2019-10-03. It is manufactured by Varian Medical Systems, Inc.. The 510(k) number is K192424.

When was Mobius3D approved by the FDA?

Mobius3D received FDA 510(k) clearance on 2019-10-03, under approval number K192424.

What company makes Mobius3D?

Mobius3D is manufactured by Varian Medical Systems, Inc..

What is the FDA product code for Mobius3D?

The FDA product code for Mobius3D is IYE.

Other Devices by Varian Medical Systems, Inc.

K162476Varian High Energy Linear Accelerator K160045Heyman Packing Applicator Set K161540Advanced Breast Template System K161576Esophagus Bougie Set K160516Universal Cylinder Applicator Family, Universal Segmented Cylinder Applicator Set, Universal Stump Applicator Set, Universal Cervix Probe Set, odd lengths, Universal Cervix Probe Set, even lengths K160021Varian Sterilization Boxes

View all 83 devices →

Related Devices (Code: IYE)

K162476Varian High Energy Linear AcceleratorVarian Medical Systems, Inc. K161400ImagingRing SystemMedphoton GmbH K162468ClearCheckRadformation K162355Raycast MammoRx Carbon Fibre Breast BoardOrfit Industries NV K162577Dosimetry Check Version 5 Release 1Math Resolutions, LLC K162265CushionCast Moldable CushionsIzi Medical Products, LLC

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.