# K024300: Microcap Plus/NPB-75

- Pathway: 510(k) (Special)
- Applicant: Oridion Medical 1987, Ltd.
- Decided: Apr 3, 2003 after 100 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 K950387 (1995). 2 ancestors in all.
20 later devices descend from it; 3 cite it directly.
0 of 23 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K964239: Combination Oximeter/Carbon Dioxide Gas Analyzer, Spegas Industries, Ltd. (1997) Summary page 1.

## Most influential descendants
- K063752: Lifesense, Model LS1-9R (2007), 12 descendants of its own
- K092101: Reusable Pulse Oximeter Sensor, Model 8000 Series (2009), 7 descendants of its own
- K040246: Fukuda Denshi Dynascope Model DS-7141 Portable Patient Monitor (2004), 4 descendants of its own
- K132402: Sensmart Model X-100 Univeral Oximetry System (2014), 3 descendants of its own
- K081891: Fukuda Denshi Dynascope Model DS-7000/7000M Patient Monitor (2008), 3 descendants of its own

## Indications for use
The MicroCap Plus /NPB-75 combined capnograph/pulse oximeter monitor is intended to provide professionally trained health care providers the continuous, non invasive measurement and monitoring of carbon dioxide concentration of the expired and inspired breath and respiration rate, and of arterial oxygen saturation (SpOn) and pulse rate.

Source page: https://510kreport.com/device/K024300
Methodology: https://510kreport.com/methodology