OCELOT CATHETER— 510(k) K123462

Name: FDA 510(k) clearance K123462
Creator: U.S. Food and Drug Administration
Published: 2012-12-07

Substantially Equivalent

Avinger, Inc.

FDA 510(k) clearance K123462 for OCELOT CATHETER, Substantially Equivalent on 2012-12-07. Applicant: Avinger, Inc.. Device class: 2.

Clearance details

Applicant: Avinger, Inc.
Product code: Code PDU
Device class: Class 2
Regulation: 21 CFR 870.1250
Advisory panel: Cardiovascular
Date received: 2012-11-09
Decision date: 2012-12-07
Decision: Substantially Equivalent
Clearance type: Special
Location: Redwood City, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code PDU

product code PDU

Malfunction: 793
Total: 793

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.