# K922927: Mortara Instrument ST Central Station

- Pathway: 510(k) (Traditional)
- Applicant: Mortara Instrument, Inc.
- Decided: Nov 10, 1992 after 146 days
- Product code: DPS (Electrocardiograph)
- Device class: 2
- Regulation: 21 CFR 870.2340
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
12 later devices descend from it; 2 cite it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K060135: Mortara Surveyor Telemetry Central Station (2006), 10 descendants of its own
- K131929: Surveyor Central Station (2013), 6 descendants of its own
- K133973: Tempus Pro with Enhanced Features (2014), 3 descendants of its own
- K170567: Tempus Pro Patient Monitor (2017), 2 descendants of its own
- K123556: Mortara Surveyor Patient Monitor (2013), 2 descendants of its own

Source page: https://510kreport.com/device/K922927
Methodology: https://510kreport.com/methodology