# K041376: C1 Series Patient Monitor, Models 863051, 863052, 863053, 863054; Optional Printer for CI, Model M3925A

- Pathway: 510(k) (Abbreviated)
- Applicant: Analogic Corp.
- Decided: Jul 20, 2004 after 57 days
- Product code: MWI (Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms))
- Device class: 2
- Regulation: 21 CFR 870.2300
- 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 K943695 (1995). 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)
- K980411: NPB3900 Series Patient Monitors, Analogic Corp. (1998) Summary page 1.

## Indications for use
The C I Series Patient Monitor series are multi-parameter patient monitors that are used to monitor ECG waveforms, heart rate, noninvasive blood pressure (systolic, dialstolic), functional arterial oxygen saturation and temperature for adult and pediatric patients in all hospital areas and health care facilities.

Source page: https://510kreport.com/device/K041376
Methodology: https://510kreport.com/methodology