DeviceSignal · 510(k) cleared
CERENOVUS, Inc.
FDA 510(k) decision recorded 2026-08-13 · K262398 · Special 510(k)
Event510(k) cleared
Effective2026-08-13
DecisionSESE
On 2026-08-13 the FDA recorded a 510(k) clearance decision for CERENOVUS, Inc., for CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing set. Clearance K262398. Product code NRY. A clearance is a regulatory decision, not an endorsement of the device.
Reported facts
- 510(k) number
- K262398
- Applicant
- CERENOVUS, Inc.
- Device
- CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing set
- Decided on
- 2026-08-13
- Received on
- 2026-07-14
- Decision
- SESE
- Clearance type
- Special
- Product code
- NRY
- Review days
- 30
Every field above is as fda_device_510k published it. Nothing on this page is our interpretation.
Provenance
- Source
- fda_device_510k
- Source record
K262398- Snapshot hash
a17b676375c92ad46cfd0c81b2c18852150764f05c544c0889e193548d652e00- Source URL
- https://download.open.fda.gov/device/510k/device-510k-0001-of-0001.json.zip
- Observed
- 2026-09-08T16:22:09.483Z
- Transform
fda_device_510k_to_clearance v1- Event rule
fda_device_510k_cleared v1- Event key
c7eabc69cb345059322e3b9ca9908b8696767ef3e8892417f91a0bf60c641264- 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)