# Percuvision, LLC

- Location (FDA's records): Gahanna, OH
- FDA decisions: 3 (2009–2011): 3 510(k) clearances
- Names in FDA's records: Percuvision, LLC (2); Percuvision (1)
- Product codes: EZL (2), FGC (1)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 1 (1 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
- The Kendal Co.: 2 (https://510kreport.com/company/kendal)
- Davlite Technologies: 1 (https://510kreport.com/company/davlite-technologies)
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)

## Its most-cited devices
- K090262: Percucath Urinary Catheter (2009), cited by 1

## Recent decisions
- K110214: Directvision Catheter, Uncoated (May 27, 2011)
- K091600: Directvision Guide System (Aug 25, 2009)
- K090262: Percucath Urinary Catheter (May 28, 2009)

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