# Inhalation Plastics

- Location (FDA's records): Chicago, IL
- FDA decisions: 7 (1988–1995): 7 510(k) clearances
- Product codes: CAI (2), BTT (2), CAH (2), CAF (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
- K945565: Spiro-Flex (Jan 13, 1995)
- K914686: Thermo-Flow Set (Apr 15, 1992)
- K901315: Aeromist II Nebulizer (Sep 10, 1990)
- K900990: Filt-R-All Bacterial/Viral Filter (Apr 19, 1990)
- K900594: Anesthesia Breathing Circuit (Mar 15, 1990)
- K896832: Filt-R-All Bacterial Filter (Jan 22, 1990)
- K874659: Sterilization of Devices by Radiation (Feb 2, 1988)

Source page: https://510kreport.com/company/inhalation-plastics
