510(k) clearance
Radius VSM and Accessories
- 510(k) number
- K260676
- Applicant
- Masimo Corporation
- Decision date
- Oct 14, 2026
- Date received
- Mar 2, 2026
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Product code
- MHX
- Device type
- Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
- Device class
- Class II
- Regulation
- 21 CFR 870.1025
- Advisory committee
- Cardiovascular
- Statement or summary
- Summary
- Third party
- N
- Location
- Irvine, CA, US