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510(k) K841489

NORELCO ELECTRONIC DIGITAL BP METER by North American Philips Corp.

K841489 is an FDA 510(k) premarket notification submitted by North American Philips Corp. for the device "NORELCO ELECTRONIC DIGITAL BP METER". The FDA issued a decision of SESP on April 10, 1984. North American Philips Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESP ()
Decision Date
April 10, 1984
Date Received
April 10, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by North American Philips Corp.

  • K842486 — ELECTRONIC DIGITAL BP METER HC 3001 (August 24, 1984)
  • K833755 — ELECTRONIC DIGITAL FEVER THERMOMETER (January 30, 1984)
  • K830715 — NORELCO VIBRATING BOARD V900 (May 25, 1983)
  • K830687 — NORELCO ELECTRONIC ANALOG BLOOD PRESS (May 18, 1983)
  • K830684 — NORELCO ELECTRONIC DIGITAL BLOOD PRESS (May 18, 1983)
  • K830686 — ANEROID BLOOD PRESSURE CUFF #HC1400 (May 18, 1983)
  • K830685 — NORELCO DELUXE DIGITAL BLOOD PRESSURE (May 18, 1983)
  • K813451 — UVA FLUORESCENT TANNING LAMPS (January 28, 1982)
  • K811891 — NORELCO MASSAGER PLUS HEAT BELT (July 20, 1981)
  • K811635 — NORELCO DIGITAL BLOOD PRESSURE METER (June 30, 1981)

FDA data resources