Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of PhilipsLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list North American Philips Corp. with 15 510(k) clearances. The most recent is a 510(k) clearance dated Aug 24, 1984: ELECTRONIC DIGITAL BP METER HC 3001.
| Aug 24, 1984 | ELECTRONIC DIGITAL BP METER HC 3001K842486 · DXN | 510(k) clearances |
| Apr 10, 1984 | NORELCO ELECTRONIC DIGITAL BP METERK841489 · | 510(k) clearances |
| Jan 30, 1984 | ELECTRONIC DIGITAL FEVER THERMOMETERK833755 · FLL | 510(k) clearances |
| May 25, 1983 | NORELCO VIBRATING BOARD V900K830715 · IRO | 510(k) clearances |
| May 18, 1983 | NORELCO DELUXE DIGITAL BLOOD PRESSUREK830685 · DXN | 510(k) clearances |
| May 18, 1983 | ANEROID BLOOD PRESSURE CUFF #HC1400K830686 · DXN | 510(k) clearances |
| May 18, 1983 | NORELCO ELECTRONIC DIGITAL BLOOD PRESSK830684 · DXN | 510(k) clearances |
| May 18, 1983 | NORELCO ELECTRONIC ANALOG BLOOD PRESSK830687 · DXN | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
