Medical device makerLabelled 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 14, 2026, FDA's public records list Pulse Time Products, Ltd. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Aug 23, 1990: BP50 BLOOD PRESSURE AND PULSE MONITOR.
| Aug 23, 1990 | BP50 BLOOD PRESSURE AND PULSE MONITORK901392 · DXN | 510(k) clearances |
| Aug 25, 1989 | PULSE TIME PRODUCTS LIMITED, PM-2K892794 · DRT | 510(k) clearances |
| Aug 25, 1989 | PULSE TIME PRODUCTS LIMITED, PM-3K892795 · DRT | 510(k) clearances |
| Jun 24, 1987 | PULSE/B.P. MONITORK864411 · DXN | 510(k) clearances |
| Mar 20, 1987 | PM-8 HEART RATE MONITORK864748 · DRT | 510(k) clearances |
| Sep 16, 1981 | CARDIACMONITORSK811425 · DRT | 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
