CARDIOQ, MODEL 9051-7005— 510(k) K031706

Substantially Equivalent

Deltex Medical

FDA 510(k) clearance K031706 for CARDIOQ, MODEL 9051-7005, Substantially Equivalent on 2003-08-06. Applicant: Deltex Medical. Device class: 2.

Clearance details

Applicant: Deltex Medical
Product code: Code DPW
Device class: Class 2
Regulation: 21 CFR 870.2100
Advisory panel: Cardiovascular
Date received: 2003-06-02
Decision date: 2003-08-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chichester, West Sussex, GB

Download summary PDF View on FDA.gov ↗

Recent devices under product code DPW

K260700 — BlueDop Vascular Expert2026-07-08
K252810 — FloPatch FP1202026-04-24
K251904 — VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-CP-01, VC-SD-01) +1 more2025-11-20
K251114 — FloPatch FP1202025-06-20
K243852 — Elfor-L2025-04-14

More clearances from Deltex Medical

K052989 — DP240 240 HOUR DOPPLER PROBE2006-03-08
K951369 — EDM1995-11-07

Data sourced from openFDA. This site is unofficial and independent of the FDA.