# Ausonics Pty, Ltd.

- Location (FDA's records): Suffield, CT
- FDA decisions: 27 (1979–1994): 27 510(k) clearances
- Product codes: IYO (12), IZH (3), ITX (3), JOP (2), DXK (1), HEM (1), JAA (1), LEJ (1), LMB (1), IYN (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
- K933916: Ausonics Opus 2 Realtime Ultrasound Scanner (Oct 3, 1994)
- K915715: Cine Recall Function/Opus 1 Real Time Scanner (Jul 2, 1992)
- K920307: Ausonics Opus 1 System, Annular Array Option (May 19, 1992)
- K905488: Doppler Upgrade for Ausonics Opus 1 Real Time Scan (Dec 18, 1991)
- K902728: 7.5 MHZ BI Plane Rectal Probe (P/N: 041-815) (Feb 13, 1991)
- K896714: Ausonics 5000 (Jun 11, 1990)
- K881979: Resubmittal of MI 1000C Microimager (Jun 12, 1989)
- K884299: Apa-C Catalog Number a-8001-C (Jan 10, 1989)

Source page: https://510kreport.com/company/ausonics