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FDA 510(k)

Alta Multipurpose Device

K-Number: K193243 · 2020-02-28

ApplicantQfix
Decision Date2020-02-28
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Alta Multipurpose Device is the device name listed in this FDA 510(k) record. The listed applicant is Qfix. It received FDA 510(k) clearance on 2020-02-28 under 510(k) number K193243. 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 Alta Multipurpose Device?

Alta Multipurpose Device is a medical device that received FDA 510(k) clearance on 2020-02-28. The listed applicant is Qfix. The 510(k) number is K193243.

When did Alta Multipurpose Device receive FDA 510(k) clearance?

Alta Multipurpose Device received FDA 510(k) clearance on 2020-02-28, under 510(k) number K193243.

Who is the listed applicant for Alta Multipurpose Device?

The FDA 510(k) record lists Qfix as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Alta Multipurpose Device?

The FDA product code for Alta Multipurpose Device is IYE.

Other records listing Qfix 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.

K230312Iris AirShuttle™K190668Encompass 15 Channel Head Coil, 3TK182189Encompass SRS Headframe ; Encompass MR SRS HeadframeK171133Qfix® Abdominal/Thoracic Motion Control System,Qfix® SBRT Solution and AccessoriesK160627Symphony Patient Transport System, Symphony Patient Trolley, Symphony Standard Transfer Surface, Symphony Portrait (Head/Neck) Transfer Surface, Symphony Brachytherapy solution

Related Devices (Code: IYE)

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.

K261856Halcyon, Ethos Radiotherapy System (5.0)Varian Medical Systems, Inc.K252937ThinkQA 3Dosisoft SAK253004LUNA 3DLap GmbH Laser ApplikationenK260792AerFrame Patient Immobilization System (AFPIS)Stabilix, LLCK252258VERIQA RT EPID 3DPtw-Freiburg Physikalisch-Technische-Werkstaetten Dr. PychlaK253962ClearCheck (RADCC V2.7)Radformation, 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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