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FDA 510(k)

DC-Air and Athlos-1 and Athlos-Air

K-Number: K211688 · 2021-07-22

ApplicantAthlos OY
Decision Date2021-07-22
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DC-Air and Athlos-1 and Athlos-Air is a medical device manufactured by Athlos OY. It received FDA 510(k) clearance on 2021-07-22 under approval number K211688. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DC-Air and Athlos-1 and Athlos-Air?

DC-Air and Athlos-1 and Athlos-Air is a medical device that received FDA 510(k) clearance on 2021-07-22. It is manufactured by Athlos OY. The 510(k) number is K211688.

When was DC-Air and Athlos-1 and Athlos-Air approved by the FDA?

DC-Air and Athlos-1 and Athlos-Air received FDA 510(k) clearance on 2021-07-22, under approval number K211688.

What company makes DC-Air and Athlos-1 and Athlos-Air?

DC-Air and Athlos-1 and Athlos-Air is manufactured by Athlos OY.

What is the FDA product code for DC-Air and Athlos-1 and Athlos-Air?

The FDA product code for DC-Air and Athlos-1 and Athlos-Air is MUH.

Related Devices (Code: MUH)

Official Source

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