# North American Philips Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 15 (1981–1984): 15 510(k) clearances
- Product codes: DXN (8), FLL (2), IRO (1), ISA (1), DXQ (1), IOB (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
- K842486: Electronic Digital BP Meter HC 3001 (Aug 24, 1984)
- K841489: Norelco Electronic Digital BP Meter (Apr 10, 1984)
- K833755: Electronic Digital Fever Thermometer (Jan 30, 1984)
- K830715: Norelco Vibrating Board V900 (May 25, 1983)
- K830685: Norelco Deluxe Digital Blood Pressure (May 18, 1983)
- K830684: Norelco Electronic Digital Blood Press (May 18, 1983)
- K830686: Aneroid Blood Pressure Cuff #HC1400 (May 18, 1983)
- K830687: Norelco Electronic Analog Blood Press (May 18, 1983)

Source page: https://510kreport.com/company/north-american-philips