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FDA 510(k)

Raycast High Precision Lung Board Solution

K-Number: K162862 · 2016-11-09

Decision Date2016-11-09
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Raycast High Precision Lung Board Solution is a medical device manufactured by Orfit Industries NV. It received FDA 510(k) clearance on 2016-11-09 under approval number K162862. 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 Raycast High Precision Lung Board Solution?

Raycast High Precision Lung Board Solution is a medical device that received FDA 510(k) clearance on 2016-11-09. It is manufactured by Orfit Industries NV. The 510(k) number is K162862.

When was Raycast High Precision Lung Board Solution approved by the FDA?

Raycast High Precision Lung Board Solution received FDA 510(k) clearance on 2016-11-09, under approval number K162862.

What company makes Raycast High Precision Lung Board Solution?

Raycast High Precision Lung Board Solution is manufactured by Orfit Industries NV.

What is the FDA product code for Raycast High Precision Lung Board Solution?

The FDA product code for Raycast High Precision Lung Board Solution is IYE.

Related Clinical Trials

Other Devices by Orfit Industries NV

Related Devices (Code: IYE)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.