PureLift Pro Edition— 510(k) K230506
Substantially EquivalentXtreem Pulse
FDA 510(k) clearance K230506 for PureLift Pro Edition, Substantially Equivalent on 2023-06-21. Applicant: Xtreem Pulse. Device class: 2.
Clearance details
- Applicant
- Xtreem Pulse
- Product code
- Code NFO
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- New York, NY, US
Recent devices under product code NFO
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