# K945071: Propaq 200 Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Protocol Systems, Inc.
- Decided: May 10, 1995 after 208 days
- Product code: DRT (Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm))
- 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
No predicates in its family tree.
281 later devices descend from it; 1 cites it directly.
1 of 282 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
- K012451: Propaq Encore Models 202, 204, 206; Propaq CS Models 242, 244, 246 (2001), 280 descendants of its own
- K032363: Zoll M Series Nibp Option (2003), 114 descendants of its own
- K033378: Vital Signs Monitor, Propaq LT (2004), 108 descendants of its own
- K061993: Equivital, Model EQ-01 (2006), 99 descendants of its own
- K113054: Equivital (2012), 71 descendants of its own

Source page: https://510kreport.com/device/K945071
Methodology: https://510kreport.com/methodology