FDA 510(k) · Masimo
K100617: MASIMO RESPONSABLE OXIMETRY SENSORS MODEL S2-25/25D; S2-20/20D (Masimo Corporation)
Masimo Corporation received FDA 510(k) K100617 for MASIMO RESPONSABLE OXIMETRY SENSORS MODEL S2-25/25D; S2-20/20D, with a decision date of May 28, 2010 (substantially equivalent).
Prescription or OTC: Unknown (no FDA document we parsed states it).
FDA facts
| FDA number | K100617 |
|---|---|
| Pathway | 510(k) |
| Applicant | Masimo Corporation |
| Device name | MASIMO RESPONSABLE OXIMETRY SENSORS MODEL S2-25/25D; S2-20/20D |
| Product code | DQA: Oximeter |
| Regulation (21 CFR) | 870.2700 |
| Device class | Class 2 |
| Date received | Mar 4, 2010 |
| Decision date | May 28, 2010 |
| Decision | Substantially Equivalent (SESE) |
| 510(k) type | Special |
Source: openFDA device 510(k) data, data through Oct 26, 2026.
Indications for use parsed from FDA documents
The Masimo Resposable Oximnetry Sensors are indicated for the continuous nonirnvasive monitoring of functional oxygen saturation of arterial hemoglobin (SP0 2) and pulse rate (measured by an SP0 2 sensor) for use with adult and pediatric patients, during both no motion and motion conditions, and for patients who are well or poorly perfused in hospitals, hospital-type facilities, mobile, and home environments. Technology
Extracted automatically from FDA's 510(k) summary. It can contain extraction errors and is not a verified quote. Read the wording in the FDA PDF before relying on it.
Predicates parsed from FDA documents
FDA numbers found next to the word "predicate" in the summary. The list can include reference devices; check the PDF for which device is the primary predicate.
ChatPPG interpretation
A 510(k) decision of "substantially equivalent" means FDA found the device as safe and effective as a legally marketed predicate. FDA's word for this is cleared, not approved. The clearance covers the device and indications in this submission; it does not extend to other features or versions of the same product that were not part of it. See FDA cleared vs approved.
Product code DQA is "Oximeter", class 2, 21 CFR 870.2700.
Our labels for filtering: claim SpO2 / pulse oximetry, sensor Finger PPG. These are heuristics, not FDA fields.