DeviceSignal · 510(k) cleared
Piraeus Medical, Inc.
FDA 510(k) decision recorded 2026-08-27 · K260751 · Traditional 510(k)
Event510(k) cleared
Effective2026-08-27
DecisionSESE
On 2026-08-27 the FDA recorded a 510(k) clearance decision for Piraeus Medical, Inc., for 35 Helix Guidewire. Clearance K260751. Product code MOF. A clearance is a regulatory decision, not an endorsement of the device.
Reported facts
- 510(k) number
- K260751
- Applicant
- Piraeus Medical, Inc.
- Device
- 35 Helix Guidewire
- Decided on
- 2026-08-27
- Received on
- 2026-03-06
- Decision
- SESE
- Clearance type
- Traditional
- Product code
- MOF
- Review days
- 174
Every field above is as fda_device_510k published it. Nothing on this page is our interpretation.
Provenance
- Source
- fda_device_510k
- Source record
K260751- 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
0893cedbfd26102860cfc2aeb33958be8034d519ec462597395efc59e3de4add- 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)