Cleared Traditional

K860775 - MEDIASTINAL AUTOTRANSFUSION SYSTEM

K860775 is an FDA 510(k) clearance for MEDIASTINAL AUTOTRANSFUSION SYSTEM, manufactured by Cardio Metrics, Inc.. The device is a Class 2 Cardiovascular device with product code DTP cleared through the Traditional 510(k) pathway after a 86-day FDA review.

K860775 · Cardio Metrics, Inc. · Cardiovascular device
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May 1986
Decision
86d
Days
Class 2
Risk

K860775 is an FDA 510(k) clearance for the MEDIASTINAL AUTOTRANSFUSION SYSTEM. Classified as Defoamer, Cardiopulmonary Bypass (product code DTP), Class II - Special Controls.

Submitted by Cardio Metrics, Inc. (Houston, US). The FDA issued a Cleared decision on May 28, 1986 after a review of 86 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.4230 - 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 Cardio Metrics, Inc. devices

FDA 510(k) Submission Details - K860775

510(k) Number K860775 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 03, 1986
Decision Date May 28, 1986
Days to Decision 86 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
39d faster than avg
Panel avg: 125d · This submission: 86d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DTP Device Classification - Class 2, Special Controls

Product Code DTP Defoamer, Cardiopulmonary Bypass
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.4230
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 - DTP Defoamer, Cardiopulmonary Bypass

All 30
Devices cleared under the same product code (DTP) and FDA review panel - the closest regulatory comparables to K860775.
CARDIOTOMY/MEDIASTINAL AUTO. RESERVOIR CATR-3500
K872167 · American Bentley · Sep 1987
THORASTAT ATR-XXXX
K870792 · Gish Biomedical, Inc. · Apr 1987
SARNS FILTERED CARDIOTOMY RESERVOIR
K860702 · 3M Health Care, Sarns · May 1986
MODIFIED MODEL SC4000(F) CARDIOTOMY RESERVOIR
K855049 · Scimed Life Systems, Inc. · Feb 1986
SHILEY 3L CARDIOTOMY RESERVOIR
K853503 · Shiley, Inc. · Nov 1985
CARDIOTOMY RESERVOIR BRS-XXX & HOLDER BRS-HXX
K851004 · Gish Biomedical, Inc. · May 1985