# K010436: Tempus 2000 Patient Monitor, Model 00-0001; Tempus Monitoring Station, Model 01-0011

- Pathway: 510(k) (Traditional)
- Applicant: Remote Diagnostic Technologies, Ltd.
- Decided: May 14, 2001 after 90 days
- Product code: DXH (Transmitters And Receivers, Electrocardiograph, Telephone)
- Device class: 2
- Regulation: 21 CFR 870.2920
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
16 later devices descend from it; 2 cite it directly.
0 of 17 devices in its family (counting itself) have 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
- K033410: Tempus 2000 Patient Monitor, Model 00-0002 (2004), 15 descendants of its own
- K082718: Tempusic Patient Monitor (2008), 14 descendants of its own
- K113105: Tempusic Patient Monitor (2011), 8 descendants of its own
- K152124: Tempus IC2 (2015), 7 descendants of its own
- K152645: Dictum Health (2016), 6 descendants of its own

Source page: https://510kreport.com/device/K010436
Methodology: https://510kreport.com/methodology