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FDA 510(k)

PureLift Pro Plus

K-Number: K221443 · 2022-10-21

ApplicantXtreem Pulse, LLC
Decision Date2022-10-21
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PureLift Pro Plus is a medical device manufactured by Xtreem Pulse, LLC. It received FDA 510(k) clearance on 2022-10-21 under approval number K221443. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PureLift Pro Plus?

PureLift Pro Plus is a medical device that received FDA 510(k) clearance on 2022-10-21. It is manufactured by Xtreem Pulse, LLC. The 510(k) number is K221443.

When was PureLift Pro Plus approved by the FDA?

PureLift Pro Plus received FDA 510(k) clearance on 2022-10-21, under approval number K221443.

What company makes PureLift Pro Plus?

PureLift Pro Plus is manufactured by Xtreem Pulse, LLC.

What is the FDA product code for PureLift Pro Plus?

The FDA product code for PureLift Pro Plus is NFO.

Other Devices by Xtreem Pulse, LLC

K173483Pure Flow External Counter-Pulsation Device K190269PureLift K243587PureLift GLOW

Related Devices (Code: NFO)

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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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