K242392
- 510(k) number
- K242392
- Device name
- PATH BGC
- Applicant
- Crossroads Neurovascular, Inc. CA · US
- Product code
- QJP — Catheter, Percutaneous, Neurovasculature
- Decision date
- 2025-05-09
- Date received
- 2024-08-12
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
510(k) Summary (official FDA PDF): K242392.pdf
Official FDA record: K242392
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.