# Meadox Surgimed, Inc.

- Location (FDA's records): Oakland, NJ
- FDA decisions: 24 (1984–1995): 24 510(k) clearances
- Product codes: KNW (4), DQX (3), FGE (3), EZN (3), FMI (2), DYB (1), FCG (1), KOD (1), LFK (1), LJE (1), GDM (1), LIT (1)
- 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
- Guidant Corp.: 1 (https://510kreport.com/company/guidant)
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)
- Vadiswire Corporation: 1 (https://510kreport.com/company/vadiswire)

## Its most-cited devices
- K942382: MS Amplatz Extra Stiff Guide Wire (1994), cited by 2
- K851647: Olbert Catheter System for Biliary Tract Dilatatio (1985), cited by 1

## Recent decisions
- K944143: MS Classique Balloon Catheter (Mar 13, 1995)
- K945061: Noprofile Olbert Catheter System (Mar 9, 1995)
- K942382: MS Amplatz Extra Stiff Guide Wire (Aug 22, 1994)
- K930201: Acecut Sutomatic Biopsy System (Jun 9, 1993)
- K911635: Meadox (R) Surgimed (R) Biopsy Gun II (Jun 20, 1991)
- K905181: NO Profile Olbert Catheter System for Urology (Mar 6, 1991)
- K904582: Quickwire - Hydrophilic Coated Guidewire (Feb 25, 1991)
- K904983: Meadox (R) Surgimed Olbert Cath Syst for Urology (Jan 30, 1991)

Source page: https://510kreport.com/company/meadox-surgimed