DeviceSignal · 510(k) cleared
Flexicare Medical Limited.
FDA 510(k) decision recorded 2026-09-02 · K254026 · Traditional 510(k)
Event510(k) cleared
Effective2026-09-02
DecisionSESE
On 2026-09-02 the FDA recorded a 510(k) clearance decision for Flexicare Medical Limited., for 3.8mm Slim ProVu Video Bronchoscope (090-02-0038U); 5.0mm Regular ProVu Video…. Clearance K254026. Product code EOQ. A clearance is a regulatory decision, not an endorsement of the device.
Reported facts
- 510(k) number
- K254026
- Applicant
- Flexicare Medical Limited.
- Device
- 3.8mm Slim ProVu Video Bronchoscope (090-02-0038U); 5.0mm Regular ProVu Video Bronchoscope (090-02-0050U); 6.0mm Large ProVu Video Bronchoscope (090-02-0060U); ProVu Video Bronchoscope 8 display (040-07-0082U)
- Decided on
- 2026-09-02
- Received on
- 2025-12-16
- Decision
- SESE
- Clearance type
- Traditional
- Product code
- EOQ
- Review days
- 260
Every field above is as fda_device_510k published it. Nothing on this page is our interpretation.
Provenance
- Source
- fda_device_510k
- Source record
K254026- Snapshot hash
20a5eca6af1b369a7deac34e4dde0974506cc835c24e3cb66b330d9671a11814- Source URL
- https://download.open.fda.gov/device/510k/device-510k-0001-of-0001.json.zip
- Observed
- 2026-09-15T12:38:10.708Z
- Transform
fda_device_510k_to_clearance v1- Event rule
fda_device_510k_cleared v1- Event key
58dc68c959fb45f1b44f9226a5eb96e4eb9cbb9c09d01dc9a269bf28cd7fa35c- 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)