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FDA 510(k)

PureLift Pro Edition

K-Number: K230506 · 2023-06-21

ApplicantXtreem Pulse
Decision Date2023-06-21
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PureLift Pro Edition is a medical device manufactured by Xtreem Pulse. It received FDA 510(k) clearance on 2023-06-21 under approval number K230506. 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 Edition?

PureLift Pro Edition is a medical device that received FDA 510(k) clearance on 2023-06-21. It is manufactured by Xtreem Pulse. The 510(k) number is K230506.

When was PureLift Pro Edition approved by the FDA?

PureLift Pro Edition received FDA 510(k) clearance on 2023-06-21, under approval number K230506.

What company makes PureLift Pro Edition?

PureLift Pro Edition is manufactured by Xtreem Pulse.

What is the FDA product code for PureLift Pro Edition?

The FDA product code for PureLift Pro Edition is 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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