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 14, 2026, FDA's public records list Micro Direct, Inc. with 9 510(k) clearances. The most recent is a 510(k) clearance dated May 19, 2004: MICRO H2 BREATH MONITORING DEVICE WITH HYDRA SOFTWARE UTILITY.
| May 19, 2004 | MICRO H2 BREATH MONITORING DEVICE WITH HYDRA SOFTWARE UTILITYK033688 · NRH | 510(k) clearances |
| Dec 1, 2003 | MICROLAB SPIROMETERK031102 · BZG | 510(k) clearances |
| Aug 27, 2003 | MICROPEAKK030586 · BZH | 510(k) clearances |
| Nov 21, 1997 | SPIROSAFE FILTERK973314 · CAH | 510(k) clearances |
| Jun 17, 1997 | MICRODL DIARYCARD SPIROMETERK965042 · BZG | 510(k) clearances |
| Jan 24, 1997 | MICRO H2K963376 · NRH | 510(k) clearances |
| Nov 1, 1996 | MICRO SPIROMETERK963035 · BZG | 510(k) clearances |
| Oct 17, 1996 | MICROCOK950197 · CCJ | 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
