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 13, 2026, FDA's public records list Copal with 5 510(k) clearances. The most recent is a 510(k) clearance dated Apr 19, 1984: DIGITAL SPHYGMOMANOMETER UA-231.
| Date | Record | Source |
|---|---|---|
| Apr 19, 1984 | DIGITAL SPHYGMOMANOMETER UA-231K832721 · DXN | 510(k) clearances |
| Apr 17, 1984 | DIGITAL SPHGMOMANOMETER UA-271K832723 · DXN | 510(k) clearances |
| Apr 17, 1984 | DIGITAL SPHYGMOMANOMETER UA-251K832722 · DXN | 510(k) clearances |
| Dec 22, 1983 | ACTIMETER UB-103K832724 · DRT | 510(k) clearances |
| Mar 25, 1982 | ELECTRONIC DIGITAL SPHYGMOMANOMETERK820300 · 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
