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 Medix Medical Electronics (U.S.A.), Inc. with 14 510(k) clearances. The most recent is a 510(k) clearance dated Jun 23, 1986: ENTERNAL INFUSER MULTIPUMP 203.
| Jun 23, 1986 | ENTERNAL INFUSER MULTIPUMP 203K861040 · FRN | 510(k) clearances |
| Jun 12, 1986 | PARENTERAL INFUSER MEDIPUMP 204K861001 · FRN | 510(k) clearances |
| Nov 18, 1985 | INSULIN PUMP INSUMAT 229K853393 · FRN | 510(k) clearances |
| Jun 27, 1985 | INFUSAFE 205 CATOLOG NO. 205.000K852433 · FLN | 510(k) clearances |
| Feb 1, 1982 | SYRINGE DRIVER 209K813562 · FRN | 510(k) clearances |
| Sep 25, 1981 | SPIROMETER 210/211K812039 · BZG | 510(k) clearances |
| Sep 25, 1981 | VENTI-MONITOR MODEL 101K812041 · CAP | 510(k) clearances |
| Sep 24, 1981 | INFANT APNEA MONITOR MODEL 100K812045 · BZQ | 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
