# Pymah Corp., Ati Div.

- Location (FDA's records): North Hollywood, CA
- FDA decisions: 3 (1989–1990): 3 510(k) clearances
- Product codes: FRC (3)
- 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)
- Steritec Products Mfg Co, Inc.: 1 (https://510kreport.com/company/steritec-products-mfg)

## Its most-cited devices
- K895704: Ati Disp. Biological Test Pack for Ethylene Oxide (1990), cited by 2

## Recent decisions
- K895704: Ati Disp. Biological Test Pack for Ethylene Oxide (Mar 8, 1990)
- K884615: Ati-Pymah Disposable Steam Biological Test Pack (Jan 19, 1989)
- K884767: Ati-Pymah Disposable Biological Test Pack (Jan 10, 1989)

Source page: https://510kreport.com/company/pymah-ati-div
