# K951246: Propaq Encore 200 Series Monitor with Neonatal Mode and Impedance Pneumography Options

- Pathway: 510(k) (Traditional)
- Applicant: Protocol Systems, Inc.
- Decided: Feb 2, 1996 after 319 days
- Product code: FLS (Monitor, Apnea, Facility Use)
- Device class: 2
- Regulation: 21 CFR 868.2377
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
430 later devices descend from it; 5 cite it directly.
1 of 431 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K031740: VSM - Vital Signs Monitor, Model 53000 Series (2003), 290 descendants of its own
- K012451: Propaq Encore Models 202, 204, 206; Propaq CS Models 242, 244, 246 (2001), 280 descendants of its own
- K063725: MP5 Intellivue Patient Monitor (2007), 175 descendants of its own
- K071426: MP2, X2, MP5, MP20, MP30, MP40, MP50, MP60, MP70, MP80, and MP90  Intellivue Patient Monitors (2007), 151 descendants of its own
- K081793: Philips MP5 and MP5T Intellivue Patient Monitors and TRX4841A Intellivue Telemetry System Transceiver (2008), 143 descendants of its own

Source page: https://510kreport.com/device/K951246
Methodology: https://510kreport.com/methodology