# Rondex Products, Inc.

- Location (FDA's records): Rockford, IL
- FDA decisions: 11 (1984–1998): 11 510(k) clearances
- Product codes: CBP (6), BTM (3), BSJ (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
- K981169: Rondex CPR Iso-Shield (May 19, 1998)
- K942671: CPR Shield (Feb 7, 1995)
- K943761: Non-Breathing Valve (Nov 10, 1994)
- K921002: Rondex Mask Models 9122/9111/9102/911102, Modified (Oct 6, 1992)
- K914195: Rondex CPR Non Rebreathing Valve #9030, Modified (Nov 8, 1991)
- K914196: Rondex Masks Models 9015/9011/901102 Modified (Nov 8, 1991)
- K902299: CPR Valve (Non-Rebreathing) Model #9030 (Oct 26, 1990)
- K902298: Oral-Nasal Mask Resuscitation and Anesthetic Gas (Aug 22, 1990)

Source page: https://510kreport.com/company/rondex-products