# K071610: Mediaid Pulse Oximeter M30 and M34

- Pathway: 510(k) (Traditional)
- Applicant: Mediaid, Inc.
- Decided: Nov 5, 2007 after 145 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: 2 generations back to K001930 (2000). 4 ancestors in all.
4 later devices descend from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K943842: Pulse Oximeter Model 305, Palco Laboratories, Inc. (1995) Summary page 1.
- K050056: Model 2500A Palmsat Pulse Oximeter, Nonin Medical, Inc. (2005) Summary page 1.

## Most influential descendants
- K100225: Pulse Oximeter Model P10 (2011), 3 descendants of its own
- K152659: V10 (2016), 2 descendants of its own
- K170497: V10 (2017), 1 descendant of its own
- K200434: V20, V20a, AVSM3 SNF (2020), 0 descendants of its own

## Indications for use
Non-invasive measurement of arterial oxygen saturation and pulse rate in hospitals, physician's office, emergency medical facilities, or at home. The model 34 can store data in memory for later review and documentation and also features a sleep mode for basic patient sleep screening.

Source page: https://510kreport.com/device/K071610
Methodology: https://510kreport.com/methodology