Cleared Traditional

K813255 - LPM/50 MEMBRANE OXYGENATOR

K813255 is the FDA 510(k) clearance for LPM/50 MEMBRANE OXYGENATOR by Travenol Laboratories, S.A.. It is a Class 2 Cardiovascular device (product code DTZ) cleared through the Traditional 510(k) pathway after a 60-day FDA review.

K813255 · Travenol Laboratories, S.A. · Cardiovascular device
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Jan 1982
Decision
60d
Days
Class 2
Risk

K813255 is an FDA 510(k) clearance for the LPM/50 MEMBRANE OXYGENATOR. Classified as Oxygenator, Cardiopulmonary Bypass (product code DTZ), Class II - Special Controls.

Submitted by Travenol Laboratories, S.A. (Mchenry, US). The FDA issued a Cleared decision on January 18, 1982 after a review of 60 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 Travenol Laboratories, S.A. devices

Submission Details

510(k) Number K813255 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 19, 1981
Decision Date January 18, 1982
Days to Decision 60 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
65d faster than avg
Panel avg: 125d · This submission: 60d
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 191
Devices cleared under the same product code (DTZ) and FDA review panel - the closest regulatory comparables to K813255.
WM. HARVEY H-1300 INFANT/PEDIATRIC BLOOD
K821477 · C.R. Bard, Inc. · Nov 1982
BLOOD OXYGENATORS #BOS-105S BOS-5S W/
K822803 · Bentley Laboratories, Inc. · Nov 1982
INTERPULSE MEMBRANE OXYGENATOR
K821216 · Extracorporeal Medical Specialities, Inc. · Jun 1982
TERUMO HOLLOW FIBER OXYGENATOR
K812660 · Terumo Medical Corp. · Dec 1981
MANIFOLD
K811004 · American Pharmaseal Div. Ahsc · May 1981
CARDIOPULMONARY BYPASS OXYGENATOR
K810505 · Cobe Laboratories, Inc. · Apr 1981