# Bard Medical Div.

- Location (FDA's records): Covington, GA
- FDA decisions: 3 (1997–1999): 3 510(k) clearances
- Product codes: MJC (1), ODC (1), EZL (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Pathway, LLC: 1 (https://510kreport.com/company/pathway)
- Amsino International, Inc.: 1 (https://510kreport.com/company/amsino-international)
- Well Lead Medical Co., Ltd.: 1 (https://510kreport.com/company/well-lead-medical)
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)

## Its most-cited devices
- K984084: Bardex Lubri-Sil Foley Catheter (1999), cited by 4

## Recent decisions
- K984136: Bardex Lubri-Sil I.C. Foley Catheter (Feb 16, 1999)
- K984084: Bardex Lubri-Sil Foley Catheter (Feb 1, 1999)
- K970110: Bard Flexible Endoscopy Injection System (651019) (Feb 19, 1997)

Source page: https://510kreport.com/company/bard-medical-div