# K954066: Miniscope MS-3

- Pathway: 510(k) (Traditional)
- Applicant: Schiller America, Inc.
- Decided: Oct 27, 1995 after 58 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.
67 later devices descend from it; 1 cites it directly.
0 of 68 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
- K990809: Cadiscope Electronic Stethoscope (1999), 66 descendants of its own
- K013434: VP-2000/1000 (2002), 46 descendants of its own
- K082357: Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Modelwatchbp Office (TWIN200). (2008), 27 descendants of its own
- K013725: Meditron II Thesterthoscope System (2002), 16 descendants of its own
- K151869: Microlife Upper Arm Automatic Digital Blood Pressure Monitor (2015), 15 descendants of its own

Source page: https://510kreport.com/device/K954066
Methodology: https://510kreport.com/methodology