# Footprint Medical

- Location (FDA's records): San Antonio, TX
- FDA decisions: 10 (2009–2013): 10 510(k) clearances
- Names in FDA's records: Footprint Medical (6); Footprint Medical, Inc. (4)
- Product codes: FOS (3), LJS (3), KNT (2), EZD (1), DYB (1)
- 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
- Argon Medical Devices, Inc.: 1 (https://510kreport.com/company/argon-medical-devices)

## Its most-cited devices
- K093026: Footprint Medical 1.9 FR Picc Introducer (2010), cited by 1

## Recent decisions
- K130507: Footprint Medical Polyurethane Picc Catheter (Jun 3, 2013)
- K120304: Footprint Medical Polyurethane Umbilical Catheter (Mar 1, 2012)
- K102548: Footprint Medical Polyurethane Feeding Tube (Nov 26, 2010)
- K093026: Footprint Medical 1.9 FR Picc Introducer (Feb 24, 2010)
- K093252: Footprint Medical Peripherally Inserted Central Catheter (Dec 17, 2009)
- K091213: Footprint Medical Umbilical Catheter, Dual Lumen (Sep 25, 2009)
- K091214: Footprint Medical Silicone Umbilical Catheter (Sep 25, 2009)
- K091488: Footprint Medical Peripherally Inserted Central Catheter, Model S1PIC1.9-C (Sep 14, 2009)

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