Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Meditec with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jul 15, 2004: NONINVASIVE BLOOD PRESSURE MONITOR, MODELS MD-880B AND MD-900T.
| Date | Record | Source |
|---|---|---|
| Jul 15, 2004 | NONINVASIVE BLOOD PRESSURE MONITOR, MODELS MD-880B AND MD-900TK041789 · DXN | 510(k) clearances |
| Sep 6, 2000 | DIGITAL BLOOD PRESSURE MONITOR, MODEL MD-550K002655 · DXN | 510(k) clearances |
| Jul 21, 1999 | FUZZY AUTOMATIC BLOOD PRESSURE MONITOR MODELS MD-750, MD-770, MD-800K992328 · DXN | 510(k) clearances |
| Feb 22, 1999 | (1) DIGITAL BLOOD PRESSURE MONITOR, MODEL MD-250; (2) FULLY AUTOMATIC BLOOD PRESSURE MONITOR, MODEL MD-700K990380 · DXN | 510(k) clearances |
| Apr 4, 1986 | MDS-83 IN DERMATOLOGICAL/PLASTIC SURGERY APPLICATIK854833 · GEX | 510(k) clearances |
| Aug 1, 1985 | MDS 83 OPHTHALMIC DYE LASER SYSTEMK852234 · HQF | 510(k) clearances |
| Apr 23, 1984 | DERMOLASK832983 · GEX | 510(k) clearances |
| Jan 24, 1983 | MODEL ML-4000 OPHTHALMIC LASER WITH FIBER OPTIC DELIVERY SYSTEMK837030 · | 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
