Cleared Traditional

K802378 - QUICK PRIME LINES

K802378 is the FDA 510(k) clearance for QUICK PRIME LINES by Bentley Laboratories, Inc.. It is a Class 2 Cardiovascular device (product code DWF) cleared through the Traditional 510(k) pathway after a 10-day FDA review.

K802378 · Bentley Laboratories, Inc. · Cardiovascular device
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Oct 1980
Decision
10d
Days
Class 2
Risk

K802378 is an FDA 510(k) clearance for the QUICK PRIME LINES, #'S BPL-12, BPL-48 &. Classified as Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass (product code DWF), Class II - Special Controls.

Submitted by Bentley Laboratories, Inc. (Mchenry, US). The FDA issued a Cleared decision on October 10, 1980 after a review of 10 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.

View all Bentley Laboratories, Inc. devices

Submission Details

510(k) Number K802378 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 30, 1980
Decision Date October 10, 1980
Days to Decision 10 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
115d faster than avg
Panel avg: 125d · This submission: 10d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 230
Devices cleared under the same product code (DWF) and FDA review panel - the closest regulatory comparables to K802378.
CARDIOPULMONARY BYPASS
K810820 · Dlp, Inc. · Apr 1981
SARNS TWO-STATE WIRE REINFORCED CATHETER
K810415 · 3M Health Care, Sarns · Mar 1981
CARDIOPULMINARY BYPASS CATHETER CANNULA
K810548 · Dlp, Inc. · Mar 1981
SARNS MEDIASTINAL AND PERICARDIAL TUBE
K792070 · 3M Health Care, Sarns · Nov 1979
SHILEY CARDIOPLEGIC SOLUTION DEL SETS
K791947 · Shiley, Inc. · Nov 1979
CARDIOPLEGIA ADMIN. SETS
K791858 · Travenol Laboratories, S.A. · Oct 1979