# K953396: Cardiovit at-1C, at-2C

- Pathway: 510(k) (Traditional)
- Applicant: Schiller America, Inc.
- Decided: Dec 19, 1995 after 152 days
- Product code: LOS
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
10 later devices descend from it; 1 cites it directly.
0 of 11 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
- K031557: Cardiovit at-102 (2004), 9 descendants of its own
- K053207: Argus, Model LCM (2006), 5 descendants of its own
- K101619: Welch Allyn 1500 Patient Monitor (2010), 4 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

Source page: https://510kreport.com/device/K953396
Methodology: https://510kreport.com/methodology