# K061896: Mediaid Disposable Non-Adhesive Sensors, Model CST050-2101N; Reusable Finger Clip SP02 Sensors, Model CST060-2101N

- Pathway: 510(k) (Traditional)
- Applicant: Mediaid, Inc.
- Decided: Apr 12, 2007 after 283 days
- Product code: DQA (Oximeter)
- Device class: 2
- Regulation: 21 CFR 870.2700
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K911191 (1991). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K994372: MODEL 120, Palco Labs, Inc. (2000) Summary page 2.
- K911191: Palco Labs Model 300 Oxygen/Pulse Monitor, Palco Laboratories, Inc. (1991) Summary page 2.
- K001930: Model 8500, Hand Held Pulse Oximeter, Model 8500, Nonin Medical, Inc. (2000) Summary page 2.
- K002690: Model 2500, Palmsat Hand Held Pulse Oximeter, Model 2500, Nonin Medical, Inc. (2000) Summary page 2.

## Indications for use
Mediaid's compatible sensors are indicated as accessories to pulse oximeters used on Pulse Oximeters manufactured by Nonin Inc for continuous, non-invasive functional arterial oxygen saturation and pulse rate monitoring in infant, pediatric, and adult patients.

Source page: https://510kreport.com/device/K061896
Methodology: https://510kreport.com/methodology