PureLift Pro Edition
K-Number: K230506 · 2023-06-21
Device Summary
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. The listed applicant is Xtreem Pulse. The 510(k) number is K230506.
When did PureLift Pro Edition receive FDA 510(k) clearance?
PureLift Pro Edition received FDA 510(k) clearance on 2023-06-21, under 510(k) number K230506.
Who is the listed applicant for PureLift Pro Edition?
The FDA 510(k) record lists Xtreem Pulse as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PureLift Pro Edition?
The FDA product code for PureLift Pro Edition is NFO.
Other records listing Xtreem Pulse 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.