SONIXGPS VASCULAR ACCESS NEEDLE KIT— 510(k) K120349

Name: FDA 510(k) clearance K120349
Creator: U.S. Food and Drug Administration
Published: 2012-04-09

Substantially Equivalent

Ultrasonix Medical Corpation

FDA 510(k) clearance K120349 for SONIXGPS VASCULAR ACCESS NEEDLE KIT, Substantially Equivalent on 2012-04-09. Applicant: Ultrasonix Medical Corpation. Device class: 2.

Clearance details

Applicant: Ultrasonix Medical Corpation
Product code: Code DRE
Device class: Class 2
Regulation: 21 CFR 870.1310
Advisory panel: Cardiovascular
Date received: 2012-02-06
Decision date: 2012-04-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Richmond, CA

Download summary PDF View on FDA.gov ↗

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Adverse events under product code DRE

product code DRE

Death: 100
Injury: 832
Malfunction: 597
Other: 3
Total: 1,532

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.