# Intertech/Ohio

- Location (FDA's records): Fort Myers, FL
- FDA decisions: 10 (1986–1989): 10 510(k) clearances
- Product codes: BZA (3), BZO (2), BTM (2), BYD (1), CAH (1), CBP (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
- K895144: Intertech Metered Dose Elbow (Oct 19, 1989)
- K890346: Intertech Universal Hydrophobic Filter (Mar 1, 1989)
- K884525: Pediatric Humidifier Tube W/ Temperature Port (Dec 16, 1988)
- K884526: Adult Resuscitator with Mask and Filter (Nov 16, 1988)
- K882204: Resuscitator Valve Assembly W/Filter (Jul 8, 1988)
- K880394: First Response Pediatric Emergency Resuscitator (Feb 29, 1988)
- K863033: Patient Gas Sampling Kit/5STAND Alone Versions (Aug 20, 1986)
- K862020: Heat/Moisture Exchanger, Hme, W/Integral Filter (Jun 30, 1986)

Source page: https://510kreport.com/company/intertech-ohio