# Broadwest Corp.

- Location (FDA's records): New York, NY
- FDA decisions: 6 (1985–1987): 6 510(k) clearances
- Product codes: IKE (2), FOX (1), FLK (1), KMH (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
- K864569: Pododigital (Feb 4, 1987)
- K864499: Podoscope (Feb 4, 1987)
- K852302: Inox Iorceps Jar (Jul 2, 1985)
- K852301: Inox Thermometer Jar (Jul 1, 1985)
- K852300: Inox IV Stand (Jun 20, 1985)
- K851307: Inox Dry Heat Sterilizer (May 9, 1985)

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