# Steripak, Ltd.

- Location (FDA's records): Northvale, NJ
- FDA decisions: 2 (1998–1998): 2 510(k) clearances
- Product codes: CAF (1), FRO (1)
- Predicates its devices cite: 2 (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 whose devices it cites most
- Autovage: 1 (https://510kreport.com/company/autovage)
- Brennen Medical, Inc.: 1 (https://510kreport.com/company/brennen-medical)

## Firms that cite its devices most
- At Squared, LLC: 1 (https://510kreport.com/company/at-squared)
- Bioderm Sciences, Inc.: 1 (https://510kreport.com/company/bioderm-sciences)
- Nephron Pharmaceuticals Corp.: 1 (https://510kreport.com/company/nephron-pharmaceuticals)

## Its most-cited devices
- K972185: 20 ML Normal Saline Topical Solution, 0.9% W/V Sodium Chloride (1998), cited by 2
- K980829: 3ML Steri-Neb Saline - 0.9% W/V Sodium Chloride Inhalation Solution Usp (1998), cited by 1

## Recent decisions
- K980829: 3ML Steri-Neb Saline - 0.9% W/V Sodium Chloride Inhalation Solution Usp (Jun 2, 1998)
- K972185: 20 ML Normal Saline Topical Solution, 0.9% W/V Sodium Chloride (Mar 5, 1998)

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