# Harris-Lake, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 7 (1976–1977): 7 510(k) clearances
- Product codes: KDP (2), BZE (1), BTT (1), GCX (1), BTI (1), CAX (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
- K761293: Respiratory Humidifier (Jan 3, 1977)
- K761294: Respiratory Blower (Jan 3, 1977)
- K761295: Resp. Air Temp. Control & Hazard Mon. (Dec 30, 1976)
- K760333: Jar, Collector for Suction Systems (Oct 27, 1976)
- K760317: Regulators, High Suction (Aug 4, 1976)
- K760316: Regulators, Low Suction (Aug 4, 1976)
- K760314: Flowmeter, Oxygen (Aug 4, 1976)

Source page: https://510kreport.com/company/harris-lake