Cleared Traditional

K873923 - INTEGRATED MEMBRANE OXYGENATOR W/CARDIO...

K873923 is the FDA 510(k) clearance for INTEGRATED MEMBRANE OXYGENATOR W/CARDIO... by American Bentley. It is a Class 2 Cardiovascular device (product code DTZ) cleared through the Traditional 510(k) pathway after a 42-day FDA review.

K873923 · American Bentley · Cardiovascular device
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Nov 1987
Decision
42d
Days
Class 2
Risk

K873923 is an FDA 510(k) clearance for the INTEGRATED MEMBRANE OXYGENATOR W/CARDIOTOMY FILTER. Classified as Oxygenator, Cardiopulmonary Bypass (product code DTZ), Class II - Special Controls.

Submitted by American Bentley (Irvine, US). The FDA issued a Cleared decision on November 6, 1987 after a review of 42 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.4350 - 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 American Bentley devices

Submission Details

510(k) Number K873923 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 25, 1987
Decision Date November 06, 1987
Days to Decision 42 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
83d faster than avg
Panel avg: 125d · This submission: 42d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DTZ Oxygenator, Cardiopulmonary Bypass
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.4350
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 - DTZ Oxygenator, Cardiopulmonary Bypass

All 123
Devices cleared under the same product code (DTZ) and FDA review panel - the closest regulatory comparables to K873923.
SCIMED MEMBRANE OXYGENATOR, MODEL 0600-2A
K883053 · Scimed Life Systems, Inc. · Sep 1988
SCIMED ULTROX TRUE MEMBRANE OXY. ULTROX I & II
K883054 · Scimed Life Systems, Inc. · Sep 1988
COBE CML3
K880021 · Cobe Laboratories, Inc. · Apr 1988
BARD(R) WM HARVEY(R) BLOOD OXYGENATOR/MODEL H-1600
K864235 · C.R. Bard, Inc. · Jan 1987
SCIMED MEMBRANE OXYGENATOR SYSTEM - ECMO
K863476 · Scimed Life Systems, Inc. · Nov 1986
MODIFIED SARNS OXYGENATOR SYSTEM
K863515 · 3M Health Care, Sarns · Nov 1986