QUANTIEN Measurement System— 510(k) K172182

Name: FDA 510(k) clearance K172182
Creator: U.S. Food and Drug Administration
Published: 2017-08-18

Substantially Equivalent

St. Jude Medical (Now Part of the Abbott Medical)

FDA 510(k) clearance K172182 for QUANTIEN Measurement System, Substantially Equivalent on 2017-08-18. Applicant: St. Jude Medical (Now Part of the Abbott Medical). Device class: 2.

Clearance details

Applicant: St. Jude Medical (Now Part of the Abbott Medical)
Product code: Code DQK
Device class: Class 2
Regulation: 21 CFR 870.1425
Advisory panel: Cardiovascular
Date received: 2017-07-19
Decision date: 2017-08-18
Decision: Substantially Equivalent
Clearance type: Special
Location: St. Paul, MN, US

Download summary PDF View on FDA.gov ↗

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K252978 — ScioCardio ECG Analysis Platform2026-07-09

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.