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 15, 2026, FDA's public records list Cooper Medical with 5 510(k) clearances. The most recent is a 510(k) clearance dated May 18, 1984: YAG LASER 8000 GASTROINTESTINAL BLEE.
| May 18, 1984 | YAG LASER 8000 GASTROINTESTINAL BLEEK840144 · FCG | 510(k) clearances |
| Apr 18, 1984 | ARGON LASER SURGICAL SYSTEM 770K833387 · | 510(k) clearances |
| Apr 17, 1984 | COOPER MEDICAL MODEL 770K833497 · LLF | 510(k) clearances |
| Jan 30, 1984 | ARGON LASER SYS-MODEL 5000K832703 · HQE | 510(k) clearances |
| Mar 5, 1982 | MONITOR CO2 LASER SYSTEMK820261 · HHR | 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
