# K001306: Stethos, Model Stxxyyzz or 001 XXX, Stethos Link, Model Slxxyyzz or 002 XXX

- Pathway: 510(k) (Traditional)
- Applicant: Andromed, Inc.
- Decided: Jul 20, 2000 after 86 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.
No later device cites it as a predicate yet.
0 of 1 device 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.

Source page: https://510kreport.com/device/K001306
Methodology: https://510kreport.com/methodology