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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 a medical device manufactured by Qfix. It received FDA 510(k) clearance on 2020-02-28 under approval 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. It is manufactured by Qfix. The 510(k) number is K193243.

When was Alta Multipurpose Device approved by the FDA?

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

What company makes Alta Multipurpose Device?

Alta Multipurpose Device is manufactured by Qfix.

What is the FDA product code for Alta Multipurpose Device?

The FDA product code for Alta Multipurpose Device is IYE.

Other Devices by Qfix

K160627Symphony Patient Transport System, Symphony Patient Trolley, Symphony Standard Transfer Surface, Symphony Portrait (Head/Neck) Transfer Surface, Symphony Brachytherapy solution K171133Qfix® Abdominal/Thoracic Motion Control System,Qfix® SBRT Solution and Accessories K182189Encompass SRS Headframe ; Encompass MR SRS Headframe K190668Encompass 15 Channel Head Coil, 3T K230312Iris AirShuttle™

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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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