Cleared Traditional

K083763 - ZEUS CT PICC 4 FR AND 5 FR SINGLE AND D...

K083763 is an FDA 510(k) clearance for ZEUS CT PICC 4 FR AND 5 FR SINGLE AND D..., manufactured by R4 Vascular, Inc.. The device is a Class 2 General Hospital device with product code LJS cleared through the Traditional 510(k) pathway after a 88-day FDA review.

K083763 · R4 Vascular, Inc. · General Hospital
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Mar 2009
Decision
88d
Days
Class 2
Risk

K083763 is an FDA 510(k) clearance for the ZEUS CT PICC 4 FR AND 5 FR SINGLE AND DUAL LUMEN. Classified as Catheter, Intravascular, Therapeutic, Long-term Greater Than 30 Days (product code LJS), Class II - Special Controls.

Submitted by R4 Vascular, Inc. (Maple Grove, US). The FDA issued a Cleared decision on March 16, 2009 after a review of 88 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5970 - the FDA general hospital 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all R4 Vascular, Inc. devices

FDA 510(k) Submission Details - K083763

510(k) Number K083763 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 18, 2008
Decision Date March 16, 2009
Days to Decision 88 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
41d faster than avg
Panel avg: 129d · This submission: 88d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LJS Device Classification - Class 2, Special Controls

Product Code LJS Catheter, Intravascular, Therapeutic, Long-term Greater Than 30 Days
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5970
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 General Hospital devices follow this clearance model.

Regulatory Peers - LJS Catheter, Intravascular, Therapeutic, Long-term Greater Than 30 Days

All 191
Devices cleared under the same product code (LJS) and FDA review panel - the closest regulatory comparables to K083763.
BD L-CATH SINGLE AND DUAL LUMENT CATHETERS, MIDLINE CATHETER
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PRO-PICC (BASIC TRAY, LONG WIRE TRAY, BASIC NURSING TRAY, FULL NURSING TRAY)
K081904 · Medcomp · Sep 2008
TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER (PICC)
K072625 · Cook, Inc. · Dec 2007
PRO-PICC, BASIC TRAY
K072509 · Medcomp · Nov 2007