Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in AustraliaLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 4 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Medical Monitors with 5 510(k) clearances. The most recent is a 510(k) clearance dated Aug 2, 2006: PEPER.
| Aug 2, 2006 | PEPERK060297 · DXH | 510(k) clearances |
| Jun 23, 2003 | PER, MODEL MEMOK030218 · DXH | 510(k) clearances |
| Jun 11, 2001 | BPFONE, MODEL UA 767ITK010751 · DXN | 510(k) clearances |
| Mar 19, 1990 | ADAM (ACOUSTICAL DEVICE FOR ANATOMICAL MONITORING)K893557 · DQD | 510(k) clearances |
| Jan 21, 1977 | AUTOMATIC ELECTRONIC SPHYGMOMANOMETERK760738 · 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
