PureLift Pro Plus
K-Number: K221443 · 2022-10-21
Device Summary
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. The listed applicant is Xtreem Pulse, LLC. The 510(k) number is K221443.
When did PureLift Pro Plus receive FDA 510(k) clearance?
PureLift Pro Plus received FDA 510(k) clearance on 2022-10-21, under 510(k) number K221443.
Who is the listed applicant for PureLift Pro Plus?
The FDA 510(k) record lists Xtreem Pulse, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PureLift Pro Plus?
The FDA product code for PureLift Pro Plus is NFO.
Other records listing Xtreem Pulse, LLC as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: NFO)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.