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 Micromedical Devices with 7 510(k) clearances. The most recent is a 510(k) clearance dated Dec 10, 2004: PALMSCAN AP2000; PALMSCAN A2000; PALMSCAN P2000.
| Dec 10, 2004 | PALMSCAN AP2000; PALMSCAN A2000; PALMSCAN P2000K043287 · IYO | 510(k) clearances |
| Aug 17, 1994 | LAPAROSCOPESK936195 · GCJ | 510(k) clearances |
| Apr 11, 1994 | ADAIR INSUFFLATION AND INSTRUMENTATION CANNULAK936155 · HIF | 510(k) clearances |
| Mar 31, 1994 | VIDEO CAMERAS, ENCOSCOPIC AND SURGICALK936097 · GCJ | 510(k) clearances |
| Mar 17, 1994 | STERILE VIDEO CAMERA COVER AND DRAPEK936086 · KXK | 510(k) clearances |
| Jun 19, 1985 | MDI 2000 - PULSE GENERATORK850791 · DRO | 510(k) clearances |
| Feb 4, 1984 | TRANS-PACEK834262 · DRO | 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
