# Advanced Instruments, Inc.

- FDA decisions: 16 (1979–2016): 16 510(k) clearances
- Product codes: JJM (7), JOW (1), JJQ (1), DQA (1), MHX (1), CIG (1), GKL (1), LMC (1), GWQ (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Edan Instruments, Inc.: 2 (https://510kreport.com/company/edan-instruments)
- Sysmex America, Inc.: 1 (https://510kreport.com/company/sysmex-america)

## Firms that cite its devices most
- Midwest Reprocessing Center, LLC: 2 (https://510kreport.com/company/midwest-reprocessing-center)
- Hygia Health Services, Inc.: 1 (https://510kreport.com/company/hygia-health-services)
- Radiometer America, Inc.: 1 (https://510kreport.com/company/radiometer-america)

## Its most-cited devices
- K930526: Intermittent Compression System Model 5000 (1993), cited by 3
- K790608: BL Bilirubinometer (1979), cited by 1

## Recent decisions
- K152776: Glocyte Automated Cell Counter System (May 27, 2016)
- K120631: Patient Monitor (May 25, 2012)
- K112465: Vital Signs Monitor (Sep 14, 2011)
- K965036: The Advanced Osmometer (3900) (Feb 20, 1997)
- K962056: Advanced Micro-Osmometer Model 3300 (Jul 11, 1996)
- K930526: Intermittent Compression System Model 5000 (Nov 18, 1993)
- K925970: Model 3D3 Osmometer (Jul 9, 1993)
- K911092: Osmometer Model 2400 (May 22, 1991)

Source page: https://510kreport.com/company/advanced-instruments