# Ongard Meddevice Packaging, Inc.

- Location (FDA's records): Denver, CO
- FDA decisions: 2 (1994–1994): 2 510(k) clearances
- Product codes: KCT (2)
- 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
- K932088: Autopak Sterilization Pouch (Nov 17, 1994)
- K932086: Autopak Instrument Tray Sterilization Pouch (Nov 17, 1994)

Source page: https://510kreport.com/company/ongard-meddevice-packaging
