Cleared Traditional

K820702 - IL 7F FLOW DIRECTOR THERMAL DILU. CATH

K820702 is an FDA 510(k) clearance for IL 7F FLOW DIRECTOR THERMAL DILU. CATH, manufactured by Instrumentation Laboratory CO. The device is a Class 2 Cardiovascular device with product code DYG cleared through the Traditional 510(k) pathway after a 37-day FDA review.

K820702 · Instrumentation Laboratory CO · Cardiovascular device
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Apr 1982
Decision
37d
Days
Class 2
Risk

K820702 is an FDA 510(k) clearance for the IL 7F FLOW DIRECTOR THERMAL DILU. CATH. Classified as Catheter, Flow Directed (product code DYG), Class II - Special Controls.

Submitted by Instrumentation Laboratory CO (Mchenry, US). The FDA issued a Cleared decision on April 21, 1982 after a review of 37 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 Instrumentation Laboratory CO devices

FDA 510(k) Submission Details - K820702

510(k) Number K820702 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 15, 1982
Decision Date April 21, 1982
Days to Decision 37 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
88d faster than avg
Panel avg: 125d · This submission: 37d
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 69
Devices cleared under the same product code (DYG) and FDA review panel - the closest regulatory comparables to K820702.
MEDTRONIC S3 TM SYSTEM
K821004 · Medtronic Vascular · May 1982
HEPARIN COATED THERMODILUTION CATHETER
K821235 · Gould, Inc. · May 1982
SEPTISLEEVE
K820883 · Argon Medical Corp. · Apr 1982
SWAN-GANZ VIP-CATHETER
K820222 · American Edwards Laboratories · Feb 1982
NORTON FLOW DIRECTED THERMODILUTION CATH
K820229 · Norton Performance Plastics Corp. · Feb 1982
FLOW-DIRECTED THERMODILUTION CATHETER
K812324 · Sorensen Research · Sep 1981