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 Cardio Metrics with 23 510(k) clearances. The most recent is a 510(k) clearance dated Oct 14, 1997: CARDIOMETRICS FLOWIRE 300 AND XT 300 DOPPLER GUIDE WIRES.
| Oct 14, 1997 | CARDIOMETRICS FLOWIRE 300 AND XT 300 DOPPLER GUIDE WIRESK972762 · DQX | 510(k) clearances |
| Aug 18, 1997 | CARDIOMETRICS WAVEWIRE/WAVEMAP PRESSURE SYSTEMK965140 · DQX | 510(k) clearances |
| Oct 25, 1996 | CARDIOMETICS FLOWIRE, SMARTWIRE DOPPLER GUIDE WIREK951567 · ITX | 510(k) clearances |
| Jul 31, 1996 | ACCUTRAC XT INTRAVASCULAR GUIDE WIRE (FLOPPY) MODEL 2403/(FLEX) MODEL 2404K961777 · DQX | 510(k) clearances |
| Feb 28, 1996 | CARDI0METRICS FLOW WIRE XT DOPPLER GUIDE MODEL 1403, 1404K955551 · DQX | 510(k) clearances |
| Nov 7, 1995 | CARDIOMETRICS ACCUTRAC INTRAVASCULAR GUIDE WIRE (MODIFICATION)K954913 · DQX | 510(k) clearances |
| Aug 29, 1995 | CARDIOMETRICS ACCUTRAC INTRAVASCULAR GUIDE WIREK952562 · DQX | 510(k) clearances |
| Sep 19, 1994 | CARDIOMETRICS FLOWIRE DOPPLER GUIDE WIREK943022 · DQX | 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
