MEDIGUIDE TECHNOLOGY— 510(k) K120301

Name: FDA 510(k) clearance K120301
Creator: U.S. Food and Drug Administration
Published: 2012-02-24

Substantially Equivalent

St. Jude Medical, Mediguide Navigation Systems

FDA 510(k) clearance K120301 for MEDIGUIDE TECHNOLOGY, Substantially Equivalent on 2012-02-24. Applicant: St. Jude Medical, Mediguide Navigation Systems. Device class: 2.

Clearance details

Applicant: St. Jude Medical, Mediguide Navigation Systems
Product code: Code DQK
Device class: Class 2
Regulation: 21 CFR 870.1425
Advisory panel: Cardiovascular
Date received: 2012-01-31
Decision date: 2012-02-24
Decision: Substantially Equivalent
Clearance type: Special
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DQK

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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

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.