DeviceSignal · 510(k) cleared
E.A.M Benelux B.V
FDA 510(k) decision recorded 2026-09-09 · K261470 · Traditional 510(k)
Event510(k) cleared
Effective2026-09-09
DecisionSESE
On 2026-09-09 the FDA recorded a 510(k) clearance decision for E.A.M Benelux B.V, for PurGuard360(QF10). Clearance K261470. Product code NHV. A clearance is a regulatory decision, not an endorsement of the device.
Reported facts
- 510(k) number
- K261470
- Applicant
- E.A.M Benelux B.V
- Device
- PurGuard360(QF10)
- Decided on
- 2026-09-09
- Received on
- 2026-05-04
- Decision
- SESE
- Clearance type
- Traditional
- Product code
- NHV
- Review days
- 128
Every field above is as fda_device_510k published it. Nothing on this page is our interpretation.
Provenance
- Source
- fda_device_510k
- Source record
K261470- 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
c89ff2ce367ae8dfe880f3978df1ae06bb0f8e5e644477445330b995fcac655a- 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)