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 Medix, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jul 22, 2004: PROTECTIV JELCO SAFETY I.V. CATHETER, MODEL 3600 SERIES.
| Date | Record | Source |
|---|---|---|
| Jul 22, 2004 | PROTECTIV JELCO SAFETY I.V. CATHETER, MODEL 3600 SERIESK041345 · FOZ | 510(k) clearances |
| Apr 1, 1994 | EASIMIST ULTRASONIC NEBULIZERK921273 · CAF | 510(k) clearances |
| Jul 24, 1992 | MEDIX NEBULIZING SYSTEM CODE NO. 2000 AND 2001K914772 · CAF | 510(k) clearances |
| Aug 29, 1985 | MEDIX ELECTRONIC NEBULIZING SYSTEMK853071 · CCQ | 510(k) clearances |
| Oct 18, 1982 | SYRINGE PUMP 209-100K822454 · FRN | 510(k) clearances |
| Apr 19, 1978 | NERVTRON-RXK780444 · GZJ | 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
