# Oec-Diasonics, Inc.

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 8 (1985–1993): 8 510(k) clearances
- Product codes: JAA (5), KQS (1), IXR (1), OXO (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Siemens Medical Solutions USA, Inc.: 1 (https://510kreport.com/company/siemens-medical-solutions-usa)

## Its most-cited devices
- K926056: 9600 Fluoroscopic Imaging System (1993), cited by 1

## Recent decisions
- K926056: 9600 Fluoroscopic Imaging System (Jan 21, 1993)
- K924879: EP 3000 (Jan 4, 1993)
- K914446: Uroview 2000, Modification (Jan 10, 1992)
- K896583: F.a.S.T. Table (Mar 1, 1990)
- K893475: Uroview II (Aug 10, 1989)
- K872022: Uroview (Jul 16, 1987)
- K864837: Modified Mainframe of Model 902 Mobile C-Arm (Jan 30, 1987)
- K843972: Angioplus-S (Jan 3, 1985)

Source page: https://510kreport.com/company/oec-diasonics