# Mini-Mitter Co., Inc.

- Location (FDA's records): Sunriver, OR
- FDA decisions: 5 (1999–2004): 5 510(k) clearances
- Product codes: GWQ (3), GWK (1), FLL (1)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 15 (2 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Vitalog Monitoring,Inc.: 1 (https://510kreport.com/company/vitalog-monitoring)
- Ambulatory Monitoring, Inc.: 1 (https://510kreport.com/company/ambulatory-monitoring)

## Firms that cite its devices most
- Respironics, Inc.: 4 (https://510kreport.com/company/respironics)
- Camntech, Ltd.: 2 (https://510kreport.com/company/camntech)
- Cambridge Temperature Concepts, Ltd.: 1 (https://510kreport.com/company/cambridge-temperature-concepts)
- Proteus Biomedical, Inc.: 1 (https://510kreport.com/company/proteus-biomedical)
- Condor Instruments Ltda. - Epp: 1 (https://510kreport.com/company/condor-instruments-ltda-epp)
- Cadi Scientific Pte.Ltd: 1 (https://510kreport.com/company/cadi-scientific)
- Cleveland Medical Devices, Inc.: 1 (https://510kreport.com/company/cleveland-medical-devices)
- Manufacturing Technology, Inc.: 1 (https://510kreport.com/company/manufacturing-technology)

## Its most-cited devices
- K983533: Actiwatch (1999), cited by 6
- K033534: Vitalsense (2004), cited by 3
- K991033: Actiwatch-Score (1999), cited by 3
- K991045: Mini-Logger Series 2000 (1999), cited by 2
- K011430: Actiware-PLMS (2001), cited by 1

## Recent decisions
- K033534: Vitalsense (Apr 22, 2004)
- K011430: Actiware-PLMS (May 31, 2001)
- K991045: Mini-Logger Series 2000 (Sep 21, 1999)
- K991033: Actiwatch-Score (Jun 23, 1999)
- K983533: Actiwatch (Mar 23, 1999)

Source page: https://510kreport.com/company/mini-mitter