# K952885: Single Lead Digital Telemetry Transmitter

- Pathway: 510(k) (Traditional)
- Applicant: Spacelabs Medical, Inc.
- Decided: Sep 26, 1995 after 95 days
- Product code: DSI (Detector And Alarm, Arrhythmia)
- Device class: 2
- Regulation: 21 CFR 870.1025
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
27 later devices descend from it; 1 cites it directly.
0 of 28 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
- K983996: Spacelabs Medical Ultraview Digital Telemtry System (1999), 26 descendants of its own
- K080192: Hypervisor VI Central Monitoring System (Including TMS) (2008), 20 descendants of its own
- K132036: Hypervisor Central Monitoring System (Including Telemetry Monitoring System, TMS-6016) (2014), 17 descendants of its own
- K150632: Hypervisor IX Monitoring System (2015), 14 descendants of its own
- K162607: BeneVision Central Monitoring System (2017), 12 descendants of its own

Source page: https://510kreport.com/device/K952885
Methodology: https://510kreport.com/methodology