HEART RATE TURBULENCE ANALYSIS TECHNOLOGIES— 510(k) K042148

Name: FDA 510(k) clearance K042148
Creator: U.S. Food and Drug Administration
Published: 2004-12-03

Substantially Equivalent

Ge Medical Syst. Information Technologies

FDA 510(k) clearance K042148 for HEART RATE TURBULENCE ANALYSIS TECHNOLOGIES, Substantially Equivalent on 2004-12-03. Applicant: Ge Medical Syst. Information Technologies. Device class: 2.

Clearance details

Applicant: Ge Medical Syst. Information Technologies
Product code: Code DQK
Device class: Class 2
Regulation: 21 CFR 870.1425
Advisory panel: Cardiovascular
Date received: 2004-08-09
Decision date: 2004-12-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milwaukee, WI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DQK

view all

K253692 — AVVIGO+ Multi-Modality Guidance System2026-08-21
K262005 — Affera Integrated Mapping System2026-08-21
K253576 — CorVista System® with PCWP Add-On2026-07-26
K262006 — EnSite X EP System2026-07-15
K252978 — ScioCardio ECG Analysis Platform2026-07-09

More clearances from Ge Medical Syst. Information Technologies

view all

K090212 — MAC 800 RESTING ECG ANALYSIS SYSTEM2009-02-19

Adverse events under product code DQK

product code DQK

Death: 10
Injury: 225
Malfunction: 2,123
Other: 2
Total: 2,360

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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