Cleared Traditional

K823451 - CLEAR CARDIOPLEJIA DELIVERY SYSTEM

K823451 is the FDA 510(k) clearance for CLEAR CARDIOPLEJIA DELIVERY SYSTEM by 3M Health Care, Sarns. It is a Class 2 Cardiovascular device (product code DTR) cleared through the Traditional 510(k) pathway after a 58-day FDA review.

K823451 · 3M Health Care, Sarns · Cardiovascular device
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Jan 1983
Decision
58d
Days
Class 2
Risk

K823451 is an FDA 510(k) clearance for the CLEAR CARDIOPLEJIA DELIVERY SYSTEM. Classified as Heat-exchanger, Cardiopulmonary Bypass (product code DTR), Class II - Special Controls.

Submitted by 3M Health Care, Sarns (Mchenry, US). The FDA issued a Cleared decision on January 14, 1983 after a review of 58 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.4240 - 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 3M Health Care, Sarns devices

Submission Details

510(k) Number K823451 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 17, 1982
Decision Date January 14, 1983
Days to Decision 58 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
67d faster than avg
Panel avg: 125d · This submission: 58d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DTR Heat-exchanger, Cardiopulmonary Bypass
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.4240
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 - DTR Heat-exchanger, Cardiopulmonary Bypass

All 78
Devices cleared under the same product code (DTR) and FDA review panel - the closest regulatory comparables to K823451.
CARDIOPLEGIA SYSTEM CCS-XXX SERIES
K833662 · Gish Biomedical, Inc. · Dec 1983
HYPOTHERMIC MYCARDIAL PROTECTION DEV
K832417 · 3M Health Care, Sarns · Oct 1983
BLOOD CARDIOPLEGIA STAINLESS STEEL COOL
K831157 · American Bentley · May 1983
JACKET & SET
K823533 · Shiley, Inc. · Dec 1982
D6ZO DISPOSABLE HEAT EXCHANGER
K813264 · Electromedics, Inc. · Jul 1982
COBE HEAT EXCHANGER RESERVOIR MODULE
K812093 · Cobe Laboratories, Inc. · Aug 1981