Cleared Traditional

K003288 - ORIGEN DUAL LUMEN CATHETER

K003288 is an FDA 510(k) clearance for ORIGEN DUAL LUMEN CATHETER, manufactured by Origen Biomedical, Inc.. The device is a Class 2 Cardiovascular device with product code DQO cleared through the Traditional 510(k) pathway after a 231-day FDA review.

K003288 · Origen Biomedical, Inc. · Cardiovascular device
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Jun 2001
Decision
231d
Days
Class 2
Risk

K003288 is an FDA 510(k) clearance for the ORIGEN DUAL LUMEN CATHETER. Classified as Catheter, Intravascular, Diagnostic (product code DQO), Class II - Special Controls.

Submitted by Origen Biomedical, Inc. (Austin, US). The FDA issued a Cleared decision on June 8, 2001 after a review of 231 days - an extended review cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1200 - the FDA cardiovascular device oversight 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 Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

View all Origen Biomedical, Inc. devices

FDA 510(k) Submission Details - K003288

510(k) Number K003288 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 20, 2000
Decision Date June 08, 2001
Days to Decision 231 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
106d slower than avg
Panel avg: 125d · This submission: 231d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DQO Device Classification - Class 2, Special Controls

Product Code DQO Catheter, Intravascular, Diagnostic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1200
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 Cardiovascular devices follow this clearance model.

Regulatory Peers - DQO Catheter, Intravascular, Diagnostic

All 360
Devices cleared under the same product code (DQO) and FDA review panel - the closest regulatory comparables to K003288.
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