DeviceSignal · 510(k) cleared
Xtreem Pulse, LLC
FDA 510(k) decision recorded 2026-09-11 · K262861 · Special 510(k)
Event510(k) cleared
Effective2026-09-11
DecisionSESE
On 2026-09-11 the FDA recorded a 510(k) clearance decision for Xtreem Pulse, LLC, for PureLift Pro Max. Clearance K262861. Product code NFO. A clearance is a regulatory decision, not an endorsement of the device.
Reported facts
- 510(k) number
- K262861
- Applicant
- Xtreem Pulse, LLC
- Device
- PureLift Pro Max
- Decided on
- 2026-09-11
- Received on
- 2026-08-13
- Decision
- SESE
- Clearance type
- Special
- Product code
- NFO
- Review days
- 29
Every field above is as fda_device_510k published it. Nothing on this page is our interpretation.
Provenance
- Source
- fda_device_510k
- Source record
K262861- Snapshot hash
a3a25028eeae44912b95531a87efac5a606d6a01c346404e56e7ec7fd97b2d35- Source URL
- https://download.open.fda.gov/device/510k/device-510k-0001-of-0001.json.zip
- Observed
- 2026-09-23T12:43:31.676Z
- Transform
fda_device_510k_to_clearance v1- Event rule
fda_device_510k_cleared v1- Event key
d364eff3d9a039d55bb1cff7f65ec6dca50afbf27124effa1406ca22af1a8f84- Signal type
device_clearance.granted
Source terms that apply
- This is not a public alerting service and must not be used to notify patients or the public
- We do not report whether a recall is still open; FDA does not maintain that after classification
- Nothing here is a medical or clinical decision aid
- Not affiliated with, endorsed by, or certified by the FDA
Data provided by the U.S. Food and Drug Administration (https://open.fda.gov)