Cleared Traditional

K020365 - 3TM MYOCARDIAL NEEDLE-TEMPERATURE PROBE

K020365 is an FDA 510(k) clearance for 3TM MYOCARDIAL NEEDLE-TEMPERATURE PROBE, manufactured by 3t Medical Systems, LLC. The device is a Class 1 Cardiovascular device with product code KRI cleared through the Traditional 510(k) pathway after a 88-day FDA review.

K020365 · 3t Medical Systems, LLC · Cardiovascular device
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May 2002
Decision
88d
Days
Class 1
Risk

K020365 is an FDA 510(k) clearance for the 3TM MYOCARDIAL NEEDLE-TEMPERATURE PROBE. Classified as Accessory Equipment, Cardiopulmonary Bypass (product code KRI), Class I - General Controls.

Submitted by 3t Medical Systems, LLC (Conifer, US). The FDA issued a Cleared decision on May 3, 2002 after a review of 88 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.4200 - 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 3t Medical Systems, LLC devices

FDA 510(k) Submission Details - K020365

510(k) Number K020365 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 04, 2002
Decision Date May 03, 2002
Days to Decision 88 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
37d faster than avg
Panel avg: 125d · This submission: 88d
Pathway characteristics
Predicate-based equivalence.

KRI Device Classification - Class 1, General Controls

Product Code KRI Accessory Equipment, Cardiopulmonary Bypass
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 870.4200
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - KRI Accessory Equipment, Cardiopulmonary Bypass

All 33
Devices cleared under the same product code (KRI) and FDA review panel - the closest regulatory comparables to K020365.
INTERFACE MODULE IDDD
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