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 Prisma Systems with 27 510(k) clearances. The most recent is a 510(k) clearance dated Mar 3, 1995: CK QVET.
| Date | Record | Source |
|---|---|---|
| Mar 3, 1995 | CK QVETK950177 · CGS | 510(k) clearances |
| Jan 27, 1995 | CHOLESTEROL QVETK943027 · CHH | 510(k) clearances |
| Dec 29, 1994 | BUN QVETK943042 · CDN | 510(k) clearances |
| Dec 29, 1994 | GLUCOSE QVETK942963 · CFR | 510(k) clearances |
| Dec 29, 1994 | LACTATE DEHYDROGENASE QVETK942964 · CFJ | 510(k) clearances |
| Dec 29, 1994 | MAGNESIUM QVETK943001 · JGJ | 510(k) clearances |
| Dec 29, 1994 | ALKALINE PHOSPHATASE (ALKP) QVETK942997 · CJE | 510(k) clearances |
| Dec 13, 1994 | AST QVETK944102 · CIT | 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
