# K961301: E-Scope Electronic Stethoscope Model 718-7120

- Pathway: 510(k) (Traditional)
- Applicant: Delphi Consulting Group
- Decided: Jun 11, 1996 after 68 days
- Product code: DQD (Stethoscope, Electronic)
- Device class: 2
- Regulation: 21 CFR 870.1875
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
112 later devices descend from it; 5 cite it directly.
0 of 113 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
- K991367: Meditron Stethoscope System (1999), 51 descendants of its own
- K013434: VP-2000/1000 (2002), 46 descendants of its own
- K072026: RNK Electronic Stethoscope (2007), 29 descendants of its own
- K082357: Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Modelwatchbp Office (TWIN200). (2008), 27 descendants of its own

Source page: https://510kreport.com/device/K961301
Methodology: https://510kreport.com/methodology