CLIRPATH TURBO PERIPHERAL CATHETERS— 510(k) K060012

Name: FDA 510(k) clearance K060012
Creator: U.S. Food and Drug Administration
Published: 2006-09-29

Substantially Equivalent

Spectranetics Corp.

FDA 510(k) clearance K060012 for CLIRPATH TURBO PERIPHERAL CATHETERS, Substantially Equivalent on 2006-09-29. Applicant: Spectranetics Corp.. Device class: 2.

Clearance details

Applicant: Spectranetics Corp.
Product code: Code PDU
Device class: Class 2
Regulation: 21 CFR 870.1250
Advisory panel: Cardiovascular
Date received: 2006-01-03
Decision date: 2006-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Colorado Springs, CO, 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.