# Pro-Pak

- Location (FDA's records): Mchenry, IL
- FDA decisions: 3 (1982–1982): 3 510(k) clearances
- Product codes: KDD (3)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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
- Crosstex Intl.: 1 (https://510kreport.com/company/crosstex-intl)

## Its most-cited devices
- K821501: Sterile Tracheostomy Care Kit (1982), cited by 1

## Recent decisions
- K821502: Sterile Suture Removal Kit (Jul 9, 1982)
- K821500: Sterile Cath Care Kit (Jun 23, 1982)
- K821501: Sterile Tracheostomy Care Kit (Jun 16, 1982)

Source page: https://510kreport.com/company/pro-pak