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 14, 2026, FDA's public records list Mega Medical, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Mar 30, 1992: MEGA AMNIOCENTESIS KIT.
| Mar 30, 1992 | MEGA AMNIOCENTESIS KITK915863 · HIO | 510(k) clearances |
| Oct 31, 1991 | MEGA ARTHROGRAM KITK913317 · FMI | 510(k) clearances |
| Oct 31, 1991 | MEGA ANGIOGRAM KITK913397 · DQO | 510(k) clearances |
| Oct 18, 1991 | MEGA CONTINUOUS EPIDURAL ANESTHESIA KITK912445 · CAZ | 510(k) clearances |
| Oct 8, 1991 | MEGA PARACENTESIS KITK913382 · KKX | 510(k) clearances |
| Sep 26, 1991 | MEGA SPINAL ANESTHESIA KITK912322 · CAZ | 510(k) clearances |
| Sep 5, 1991 | MEGA PERICARDIOCENTESIS KITK912564 · DQY | 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
