Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United KingdomLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Deltex Medical with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jun 28, 2018: Deltex Medical CardioQ-EDM+, Deltex Medical CardioQ-EDM.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jun 28, 2018 | Deltex Medical CardioQ-EDM+, Deltex Medical CardioQ-EDMK172457 · DPW | 510(k) clearances |
| Jul 24, 2015 | Deltex Medical CardioQ-EDM, Deltex Medical CardioQ-EDM+K150347 · DPW | 510(k) clearances |
| Jan 22, 2015 | Deltex Medical KDP72 Doppler ProbeK142932 · DPT | 510(k) clearances |
| Oct 10, 2013 | DELTEX MEDICAL CARDIOQ-EDM+K132139 · DPW | 510(k) clearances |
| Oct 20, 2011 | DELTEX MEDICAL CARDIOQ EDMK111542 · DPW | 510(k) clearances |
| Jan 29, 2009 | I2S DOPPLER PROBE ( 6 HOUR), I2S DOPPLER PROBE (24 HOUR), I2C DOPPLER PROBE (72 HOUR), MODELS 9090-7015, 9090-7016K073593 · DPT | 510(k) clearances |
| Mar 8, 2006 | DP240 240 HOUR DOPPLER PROBEK052989 · DPT | 510(k) clearances |
| Aug 6, 2003 | CARDIOQ, MODEL 9051-7005K031706 · DPW | 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
