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 13, 2026, FDA's public records list Medi-Tech, Inc. with 36 510(k) clearances. The most recent is a 510(k) clearance dated May 15, 1996: MEDI-TECH EDDY INTRAVASCULAR INFUSION CATHETER.
| Date | Record | Source |
|---|---|---|
| May 15, 1996 | MEDI-TECH EDDY INTRAVASCULAR INFUSION CATHETERK954457 · KRA | 510(k) clearances |
| Aug 17, 1995 | MEDI-TECH PLATFORM GUIDE CATHETERK952345 · DQY | 510(k) clearances |
| Jun 1, 1995 | IMMUNOASSAY DRUGS OF ABUSE CONTROLSK952056 · DIF | 510(k) clearances |
| Dec 13, 1994 | DOA - IMMUNOASSAY CUT-OFF CALIBRATORK945289 · DKB | 510(k) clearances |
| Oct 6, 1994 | THERAPEUTIC DRUG MONITORING CONTROL, ASSAYEDK942551 · DIF | 510(k) clearances |
| Sep 14, 1994 | BILIRUBIN PLUS/PEDIATRIC CONTROLSK943290 · JJY | 510(k) clearances |
| Sep 12, 1994 | HEMODIALYSIS BATHK922990 · KPO | 510(k) clearances |
| Sep 9, 1994 | THERAPEUTIC DRUG MONITORING CONTROL, UNASSAYEDK942552 · DIF | 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
