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 Andromed with 5 510(k) clearances. The most recent is a 510(k) clearance dated Sep 30, 2005: ANDROFLOW - RESPIRATORY RATE MONITOR.
| Date | Record | Source |
|---|---|---|
| Sep 30, 2005 | ANDROFLOW - RESPIRATORY RATE MONITORK051779 · BZQ | 510(k) clearances |
| Oct 1, 2002 | I-STETHOS LINKK022298 · DQD | 510(k) clearances |
| Oct 1, 2002 | BIOLOGICAL SOUND MONITOR (BSM) SENSORK021389 · DQD | 510(k) clearances |
| Oct 26, 2001 | AGILENT ELECTRONIC STETHOSCOPE, MODELS M4532A AND M4533AK010729 · DQD | 510(k) clearances |
| Jul 20, 2000 | STETHOS, MODEL STXXYYZZ OR 001 XXX, STETHOS LINK, MODEL SLXXYYZZ OR 002 XXXK001306 · DQD | 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
