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 Merrimack Laboratories with 6 510(k) clearances. The most recent is a 510(k) clearance dated Feb 19, 1985: CARBON DIOXIDE LASER ML 825.
| Feb 19, 1985 | CARBON DIOXIDE LASER ML 825K833528 · HHR | 510(k) clearances |
| Feb 10, 1984 | ENDOSCOPIC COUPLERK833483 · EOQ | 510(k) clearances |
| Sep 13, 1982 | MODEL ML-850K827963 · | 510(k) clearances |
| Jun 11, 1982 | MODEL ML-820 CARBON DIOXIDE LASER SYSTEM FOR SURGERYK827506 · | 510(k) clearances |
| May 19, 1982 | ML-810 CARBON DIOXIDE LASER SYSTEMK827442 · | 510(k) clearances |
| Mar 3, 1980 | ML-800 CO2K800227 · 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
