Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of PhilipsLabelled 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 Mini-Mitter with 5 510(k) clearances. The most recent is a 510(k) clearance dated Apr 22, 2004: VITALSENSE.
| Date | Record | Source |
|---|---|---|
| Apr 22, 2004 | VITALSENSEK033534 · FLL | 510(k) clearances |
| May 31, 2001 | ACTIWARE-PLMSK011430 · GWQ | 510(k) clearances |
| Sep 21, 1999 | MINI-LOGGER SERIES 2000K991045 · GWK | 510(k) clearances |
| Jun 23, 1999 | ACTIWATCH-SCOREK991033 · GWQ | 510(k) clearances |
| Mar 23, 1999 | ACTIWATCHK983533 · GWQ | 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
