Cleared Traditional

K131060 - CLEARGUARD HD END CAP (FDA 510(k) Clearance)

Class II Gastroenterology & Urology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K131060 · Pursuit Vascular, Inc. · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Dec 2013
Decision
244d
Days
Class 2
Risk

K131060 is an FDA 510(k) clearance for the CLEARGUARD HD END CAP. Classified as Hemodialysis Catheter Luer End Cap (product code PEH), Class II - Special Controls.

Submitted by Pursuit Vascular, Inc. (Maple Grove, US). The FDA issued a Cleared decision on December 16, 2013 after a review of 244 days - an extended review cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5540 - the FDA gastroenterology and urology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Gastroenterology & Urology review framework, consistent with the majority of Class II 510(k) submissions.

View all Pursuit Vascular, Inc. devices

Submission Details

510(k) Number K131060 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 16, 2013
Decision Date December 16, 2013
Days to Decision 244 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
114d slower than avg
Panel avg: 130d · This submission: 244d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code PEH Hemodialysis Catheter Luer End Cap
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5540
Definition For Use In Hemodialysis Catheters To Reduce Hub Infection.
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Gastroenterology & Urology devices follow this clearance model.