# Ati

- Location (FDA's records): Los Angeles, CA
- FDA decisions: 3 (1989–1990): 3 510(k) clearances
- Product codes: ILO (2), FRC (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Sgm Biomedical, Inc.: 1 (https://510kreport.com/company/sgm-biomedical)
- Sgm Biotech, Inc.: 1 (https://510kreport.com/company/sgm-biotech)

## Its most-cited devices
- K902344: Ati Disposable Biological Test Pack for Steam Ster (1990), cited by 2

## Recent decisions
- K902344: Ati Disposable Biological Test Pack for Steam Ster (Jul 19, 1990)
- K890853: Aqua-Pad for Moist or Dry Heat Therapy (Apr 14, 1989)
- K890852: Aqua-Blanket Hyper/Hypohermia Blanket (Apr 14, 1989)

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