# Echo Ultrasound

- Location (FDA's records): Lewistown, PA
- FDA decisions: 6 (1985–1993): 6 510(k) clearances
- Product codes: DXK (1), IYO (1), DQC (1), DYO (1), GXX (1), JOT (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K924054: Phonocardiograph (Jan 22, 1993)
- K903414: Transesophageal Probe Holder & Disinfecting Column (Sep 19, 1990)
- K893225: Couplant Warming Device (Oct 12, 1989)
- K872519: Sterilized Omni Gel (Aug 3, 1987)
- K844034: Sonocare (Jan 23, 1985)
- K844120: Ultrasonic Scanner Calibration & Test Objects (Jan 23, 1985)

Source page: https://510kreport.com/company/echo-ultrasound