# Ameco Medical Industries

- Location (FDA's records): Monroe, CT
- FDA decisions: 6 (2011–2016): 6 510(k) clearances
- Product codes: MSD (2), LJS (1), MPB (1), DYB (1), FOZ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K152819: Amecath Peripheral inserted Central Venous Catheter Sets (Feb 5, 2016)
- K131144: Ameco Sheath Introducer (Aug 15, 2013)
- K131814: Amecath Dual Lumen Implanted Hemodialysis Catheter (Jul 26, 2013)
- K123943: Amecath Dual Lumen Hemodialysis Catheter (Apr 2, 2013)
- K110794: Amecath CVC and Amecath Pressure CVC Short Term Single and Multi-Lumen Catherization Kits (Dec 21, 2011)
- K110793: Amecath and Amecath Uniqath Soft Short Term Dual Hemodialysis Catheterization Kits (Dec 16, 2011)

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