Cleared Traditional

K951088 - QUEST RETROGRADE CARDIPLEGIA CANNULA-RCCS

K951088 is an FDA 510(k) clearance for QUEST RETROGRADE CARDIPLEGIA CANNULA-RCCS, manufactured by Quest Medical, Inc.. The device is a Class 2 Cardiovascular device with product code DWF cleared through the Traditional 510(k) pathway after a 97-day FDA review.

K951088 · Quest Medical, Inc. · Cardiovascular device
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Jun 1995
Decision
97d
Days
Class 2
Risk

K951088 is an FDA 510(k) clearance for the QUEST RETROGRADE CARDIPLEGIA CANNULA-RCCS. Classified as Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass (product code DWF), Class II - Special Controls.

Submitted by Quest Medical, Inc. (Allen, US). The FDA issued a Cleared decision on June 14, 1995 after a review of 97 days - within the typical 510(k) review window.

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: 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 Quest Medical, Inc. devices

FDA 510(k) Submission Details - K951088

510(k) Number K951088 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 09, 1995
Decision Date June 14, 1995
Days to Decision 97 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
28d faster than avg
Panel avg: 125d · This submission: 97d
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 330
Devices cleared under the same product code (DWF) and FDA review panel - the closest regulatory comparables to K951088.
HEARTPORT ENDOARTERIAL RETURN CANNUAL
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K953945 · Dlp, Inc. · Mar 1996
FOAMSEAL RETROGRADE CARDIOPLEGIA CATHETER
K955818 · Quest Medical, Inc. · Mar 1996
AORTIC ARCH CANNULAS
K943934 · Sorin Group Italia S.R.L. · Jun 1995
QUEST ANTEGRADE CARDIOPLEGIA CANNULA
K950814 · Quest Medical, Inc. · May 1995
QUEST CORONARY SINUS PERFUSION CANNULA -FRCC
K941916 · Quest Medical, Inc. · Apr 1995