Is MightySat® Fingertip Pulse Oximeter FDA approved or cleared?
Yes. MightySat® Fingertip Pulse Oximeter by Masimo Corporation is named in the FDA register with a 510(k) clearance, first authorised in 2015, latest decision in 2024.
In the EU: CE class IIb, found in EUDAMED. The manufacturer holds a valid notified body certificate under the MDR in EUDAMED.
At a glance
| Product | MightySat® Fingertip Pulse Oximeter |
|---|---|
| Maker | Masimo Corporation |
| Care area | Vital signs & remote monitoring |
| What it does | Fingertip pulse oximeter with advanced signal processing technology |
| FDA | 510(k), latest decision 2024 |
| Verification level | Exact product named in the FDA record (checked 18 October 2026) |
| EU (CE) | Class IIb |
| EU certificate | Manufacturer certificate from a notified body (MDR) in EUDAMED (checked 18 October 2026) |
| Website | masimo.com |
| Status | FDA verified |
| Last checked | 6 October 2026 |
Need the evidence behind this entry?
Certified Health Apps Pro gives you the FDA reference number, decision date and a direct link to the official record, plus the EU certificate and notified body, for every app. See Pro · Free guide: how to check a health app in two minutes
Certified Health Apps Pro gives you the FDA reference number, decision date and a direct link to the official record, plus the EU certificate and notified body, for every app. See Pro · Free guide: how to check a health app in two minutes