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FDA 510(k)

PureLift GLOW

K-Number: K243587 · 2025-03-06

ApplicantXtreem Pulse, LLC
Decision Date2025-03-06
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PureLift GLOW is a medical device manufactured by Xtreem Pulse, LLC. It received FDA 510(k) clearance on 2025-03-06 under approval number K243587. 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 GLOW?

PureLift GLOW is a medical device that received FDA 510(k) clearance on 2025-03-06. It is manufactured by Xtreem Pulse, LLC. The 510(k) number is K243587.

When was PureLift GLOW approved by the FDA?

PureLift GLOW received FDA 510(k) clearance on 2025-03-06, under approval number K243587.

What company makes PureLift GLOW?

PureLift GLOW is manufactured by Xtreem Pulse, LLC.

What is the FDA product code for PureLift GLOW?

The FDA product code for PureLift GLOW is NFO.

Other Devices by Xtreem Pulse, LLC

K173483Pure Flow External Counter-Pulsation Device K190269PureLift K221443PureLift Pro Plus

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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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