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FDA 510(k)

RayPilot System

K-Number: K203722 · 2021-09-02

ApplicantMicropos Medical AB
Decision Date2021-09-02
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RayPilot System is a medical device manufactured by Micropos Medical AB. It received FDA 510(k) clearance on 2021-09-02 under approval number K203722. 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 RayPilot System?

RayPilot System is a medical device that received FDA 510(k) clearance on 2021-09-02. It is manufactured by Micropos Medical AB. The 510(k) number is K203722.

When was RayPilot System approved by the FDA?

RayPilot System received FDA 510(k) clearance on 2021-09-02, under approval number K203722.

What company makes RayPilot System?

RayPilot System is manufactured by Micropos Medical AB.

What is the FDA product code for RayPilot System?

The FDA product code for RayPilot System is IYE.

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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.

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