# Medi-Plast Intl., Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 12 (1981–1996): 12 510(k) clearances
- Product codes: KPE (4), DTL (2), FRG (1), FMF (1), DRE (1), FSM (1), JAA (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: 5 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Medical Specialty Innovations, Inc. (Msi): 4 (https://510kreport.com/company/medical-specialty-innovations-msi)

## Its most-cited devices
- K811234: I.V. Bottle (Ridgid) (1981), cited by 1
- K811233: I.V. Plastic Bag (1981), cited by 1
- K811268: Bottle-to-Bottle (1981), cited by 1
- K811269: Glass Vials (1981), cited by 1

## Recent decisions
- K954284: Medi-Plast 2 Port Manifold (Right on) (Feb 12, 1996)
- K873588: 10CC Control Syringe (Oct 23, 1987)
- K863402: Medi-Plast Disposable Manifold (Oct 22, 1986)
- K861785: Fluoroscope Band Bag (Jun 13, 1986)
- K851489: Arterial-Venous Compression Dressing (Jun 11, 1985)
- K842136: Sterile Pan Set (Jul 6, 1984)
- K840021: Operating Room Tray Set (Mar 15, 1984)
- K840022: Heart Catheterization Tray Set (Feb 4, 1984)

Source page: https://510kreport.com/company/medi-plast-intl