# Strom Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 3 (1981–1982): 3 510(k) clearances
- Product codes: BYI (3)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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
- Med Systems: 3 (https://510kreport.com/company/med-systems)

## Its most-cited devices
- K821570: Pneumo Pulssor Iii (1982), cited by 1
- K821265: Pneumopulssor (PPS II) (1982), cited by 1
- K813438: Pneumo Pulssor (1981), cited by 1

## Recent decisions
- K821265: Pneumopulssor (PPS II) (Jul 26, 1982)
- K821570: Pneumo Pulssor Iii (Jun 3, 1982)
- K813438: Pneumo Pulssor (Dec 29, 1981)

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