Cleared Traditional

K802879 - BUCKBERG-SHILEY BLOOD CARDIOPLEGIC SPL.

K802879 is an FDA 510(k) clearance for BUCKBERG-SHILEY BLOOD CARDIOPLEGIC SPL., manufactured by Shiley, Inc.. The device is a Class 2 Cardiovascular device with product code DTR cleared through the Traditional 510(k) pathway after a 32-day FDA review.

K802879 · Shiley, Inc. · Cardiovascular device
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Dec 1980
Decision
32d
Days
Class 2
Risk

K802879 is an FDA 510(k) clearance for the BUCKBERG-SHILEY BLOOD CARDIOPLEGIC SPL.. Classified as Heat-exchanger, Cardiopulmonary Bypass (product code DTR), Class II - Special Controls.

Submitted by Shiley, Inc. (Mchenry, US). The FDA issued a Cleared decision on December 19, 1980 after a review of 32 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 Shiley, Inc. devices

FDA 510(k) Submission Details - K802879

510(k) Number K802879 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 17, 1980
Decision Date December 19, 1980
Days to Decision 32 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
93d faster than avg
Panel avg: 125d · This submission: 32d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DTR Device Classification - Class 2, Special Controls

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 82
Devices cleared under the same product code (DTR) and FDA review panel - the closest regulatory comparables to K802879.
COBE HEAT EXCHANGER RESERVOIR MODULE
K812093 · Cobe Laboratories, Inc. · Aug 1981
BRONCHEK-SHILEY CARDIAC JACKET & BSC J
K811204 · Shiley, Inc. · May 1981
CARDIOPLEGIC SETS
K802545 · Texas Medical Products, Inc. · Jan 1981
CARDIOPLEGIA COOLING SYST. CCAS-2
K802848 · Bentley Laboratories, Inc. · Dec 1980
TOPICAL COOLING DEV. TCD. #27-999
K800717 · Cobe Laboratories, Inc. · Apr 1980
CARDIOPLEGIA DELIVERY SYSTEM
K800377 · 3M Health Care, Sarns · Mar 1980