# Tandem Medical, Inc.

- Location (FDA's records): San Diego, CA
- FDA decisions: 2 (1999–2000): 2 510(k) clearances
- Product codes: MEB (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Solopak Medical Products, Inc.: 1 (https://510kreport.com/company/solopak-medical-products)
- I-Flow Corp.: 1 (https://510kreport.com/company/i-flow)

## Its most-cited devices
- K990889: Autodose Infusion System (1999), cited by 1

## Recent decisions
- K993832: Autodose Infusion System, Model AD4120, BE4210, S12050,100,200, FF0005, 10 (Feb 9, 2000)
- K990889: Autodose Infusion System (Jun 3, 1999)

Source page: https://510kreport.com/company/tandem-medical