Cleared Traditional

K802481 - 7FRENCH FLOW DIRECTED TRIPLE LUMEN CATH

K802481 is an FDA 510(k) clearance for 7FRENCH FLOW DIRECTED TRIPLE LUMEN CATH, manufactured by Waters Assoc., Inc.. The device is a Class 2 Cardiovascular device with product code DYG cleared through the Traditional 510(k) pathway after a 24-day FDA review.

K802481 · Waters Assoc., Inc. · Cardiovascular device
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Oct 1980
Decision
24d
Days
Class 2
Risk

K802481 is an FDA 510(k) clearance for the 7FRENCH FLOW DIRECTED TRIPLE LUMEN CATH. Classified as Catheter, Flow Directed (product code DYG), Class II - Special Controls.

Submitted by Waters Assoc., Inc. (Mchenry, US). The FDA issued a Cleared decision on October 31, 1980 after a review of 24 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1240 - 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 Waters Assoc., Inc. devices

FDA 510(k) Submission Details - K802481

510(k) Number K802481 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 07, 1980
Decision Date October 31, 1980
Days to Decision 24 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
101d faster than avg
Panel avg: 125d · This submission: 24d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DYG Device Classification - Class 2, Special Controls

Product Code DYG Catheter, Flow Directed
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1240
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 - DYG Catheter, Flow Directed

All 70
Devices cleared under the same product code (DYG) and FDA review panel - the closest regulatory comparables to K802481.
SWAN-GANZ FLOW-DIRECTED THERMODILUTION
K810352 · American Edwards Laboratories · Mar 1981
SWAN-GANZ VIP THERMODILUTION CATHETER
K810124 · American Edwards Laboratories · Feb 1981
SWAN GANZ CATHETER PLACEMENT KIT
K802288 · Stanco Medical, Inc. · Nov 1980
TORQUE CONTROL BALLOON CATHETER
K802338 · Cordis Corp. · Oct 1980
CORDIS FLOW DIRECTED BALLOON CATHETER
K801865 · Cordis Corp. · Aug 1980
CATHETER, USCI GRUNTZIG/BALLOON
K782071 · C.R. Bard, Inc. · Dec 1978