North American Philips Corp.
North American Philips Corp. holds FDA 510(k) medical device clearances, first cleared 1981, most recent 1984.
Top product codes for North American Philips Corp.
Recent clearances by North American Philips Corp.
- K842486 — ELECTRONIC DIGITAL BP METER HC 3001
- K841489 — NORELCO ELECTRONIC DIGITAL BP METER
- K833755 — ELECTRONIC DIGITAL FEVER THERMOMETER
- K830715 — NORELCO VIBRATING BOARD V900
- K830684 — NORELCO ELECTRONIC DIGITAL BLOOD PRESS
- K830685 — NORELCO DELUXE DIGITAL BLOOD PRESSURE
- K830686 — ANEROID BLOOD PRESSURE CUFF #HC1400
- K830687 — NORELCO ELECTRONIC ANALOG BLOOD PRESS
- K813451 — UVA FLUORESCENT TANNING LAMPS
- K811891 — NORELCO MASSAGER PLUS HEAT BELT
- K811634 — NORELCO ANEROID BLOOD PRESSURE METER
- K811635 — NORELCO DIGITAL BLOOD PRESSURE METER
- K811636 — NORELCO ELECTRONIC BLOOD PRESSURE METER
- K811672 — NORELCO ELECTRONIC DIGITAL THERMOMETER
- K811188 — NORELCO BLOOD PRESSURE METER
Data sourced from openFDA. This site is unofficial and independent of the FDA.