Cleared Traditional

K882137 - EXTENDED SHELF LIFE FOR INTERSEPT* ARTE...

K882137 is the FDA 510(k) clearance for EXTENDED SHELF LIFE FOR INTERSEPT* ARTE... by Medtronic Blood Systems, Inc.. It is a Class 2 Cardiovascular device (product code DTM) cleared through the Traditional 510(k) pathway after a 84-day FDA review.

K882137 · Medtronic Blood Systems, Inc. · Cardiovascular device
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Aug 1988
Decision
84d
Days
Class 2
Risk

K882137 is an FDA 510(k) clearance for the EXTENDED SHELF LIFE FOR INTERSEPT* ARTERIAL 20/40. Classified as Filter, Blood, Cardiopulmonary Bypass, Arterial Line (product code DTM), Class II - Special Controls.

Submitted by Medtronic Blood Systems, Inc. (Anaheim, US). The FDA issued a Cleared decision on August 12, 1988 after a review of 84 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.4260 - 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 Medtronic Blood Systems, Inc. devices

Submission Details

510(k) Number K882137 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 20, 1988
Decision Date August 12, 1988
Days to Decision 84 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
41d faster than avg
Panel avg: 125d · This submission: 84d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DTM Filter, Blood, Cardiopulmonary Bypass, Arterial Line
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.4260
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 - DTM Filter, Blood, Cardiopulmonary Bypass, Arterial Line

All 59
Devices cleared under the same product code (DTM) and FDA review panel - the closest regulatory comparables to K882137.
MODIFIED PYROGEN TESTING
K910935 · Electromedics, Inc. · May 1991
ARTERIAL BLOOD FILTER ELECTRO. AIR* STAR 40 AND 20
K902723 · Electromedics, Inc. · Dec 1990
HEPARINIZED ARTERIAL SCREEN BLOOD FILTER
K900758 · Cobe Laboratories, Inc. · May 1990
ARTERIAL 20/40 MICRON FILTERS W/WO HEPARIN COATING
K864262 · Johnson & Johnson Professionals, Inc. · Jan 1987
SWANK ARTERIAL LINE BLOOD FILTER HF6000
K855066 · Cobe Laboratories, Inc. · Feb 1986
ARTERIAL FILTER AFS-XX /FILTER HOLDER AFS-HXX
K851003 · Gish Biomedical, Inc. · Jul 1985