K243503
- 510(k) number
- K243503
- Device name
- VIA360 Surgical System
- Applicant
- New World Medical, Inc. CA · US
- Product code
- MRH — Pump, Infusion, Ophthalmic
- Decision date
- 2025-02-14
- Date received
- 2024-11-12
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
510(k) Summary (official FDA PDF): K243503.pdf
Official FDA record: K243503
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.