Cleared Traditional

K022321 - STOCKERT V172-28 VENOUS FEMORAL CANNULA

K022321 is an FDA 510(k) clearance for STOCKERT V172-28 VENOUS FEMORAL CANNULA, manufactured by Stockert Instrumente GmbH. The device is a Class 2 Cardiovascular device with product code DWF cleared through the Traditional 510(k) pathway after a 84-day FDA review.

K022321 · Stockert Instrumente GmbH · Cardiovascular device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Oct 2002
Decision
84d
Days
Class 2
Risk

K022321 is an FDA 510(k) clearance for the STOCKERT V172-28 VENOUS FEMORAL CANNULA. Classified as Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass (product code DWF), Class II - Special Controls.

Submitted by Stockert Instrumente GmbH (Arvada, US). The FDA issued a Cleared decision on October 9, 2002 after a review of 84 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.4210 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

FDA 510(k) Submission Details - K022321

510(k) Number K022321 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 17, 2002
Decision Date October 09, 2002
Days to Decision 84 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
41d faster than avg
Panel avg: 125d · This submission: 84d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DWF Device Classification - Class 2, Special Controls

Product Code DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.4210
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 - DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

All 397
Devices cleared under the same product code (DWF) and FDA review panel - the closest regulatory comparables to K022321.
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K022042 · Cardeon Corp. · Sep 2002
K022321 · STOCKERT V172-28 VENOUS FEMORAL CANNULA
Download PDF FDA Summary Stockert Instrumente …