# Megaplast, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 7 (1981–1982): 7 510(k) clearances
- Product codes: KDD (2), FJZ (1), KOD (1), KNX (1), KYZ (1), KNT (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
- K822158: Open Heart Tray (Custom Designed) (Oct 13, 1982)
- K821313: Surgical Utility Drape (Jun 21, 1982)
- K820423: Suture Removal Tray (Mar 10, 1982)
- K820136: Urinary Drainage Bag (Jan 29, 1982)
- K810249: Tray, Catherization, Urethral (Apr 7, 1981)
- K810250: Tray, Irrigation (Apr 7, 1981)
- K810251: Syringe, Ent (Mar 11, 1981)

Source page: https://510kreport.com/company/megaplast