K242504
- 510(k) number
- K242504
- Device name
- Millipede 088 Access Catheter; Millipede 070 Aspiration Catheter; Perfuze Aspiration Tube Set
- Applicant
- Perfuze, Ltd. IE
- Product code
- NRY — Catheter, Thrombus Retriever
- Decision date
- 2024-09-20
- Date received
- 2024-08-22
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
510(k) Summary (official FDA PDF): K242504.pdf
Official FDA record: K242504
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.