FLOCONTROL , MODEL 1028— 510(k) K090970

Name: FDA 510(k) clearance K090970
Creator: U.S. Food and Drug Administration
Published: 2009-06-12

Substantially Equivalent

Coaxia, Inc.

FDA 510(k) clearance K090970 for FLOCONTROL , MODEL 1028, Substantially Equivalent on 2009-06-12. Applicant: Coaxia, Inc.. Device class: 2.

Clearance details

Applicant: Coaxia, Inc.
Product code: Code MJN
Device class: Class 2
Regulation: 21 CFR 870.4450
Advisory panel: Cardiovascular
Date received: 2009-04-06
Decision date: 2009-06-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Maple Grove, MN, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code MJN

product code MJN

Death: 31
Injury: 240
Malfunction: 827
Total: 1,098

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.