Cleared Traditional

K904171 - SCIMED CARDIOTHERM CARDIOPLEGIA DELIVERY SYSTEM

K904171 is an FDA 510(k) clearance for SCIMED CARDIOTHERM CARDIOPLEGIA DELIVER..., manufactured by Scimed. The device is a Class 2 Cardiovascular device with product code DTR cleared through the Traditional 510(k) pathway after a 86-day FDA review.

K904171 · Scimed · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Dec 1990
Decision
86d
Days
Class 2
Risk

K904171 is an FDA 510(k) clearance for the SCIMED CARDIOTHERM CARDIOPLEGIA DELIVERY SYSTEM. Classified as Heat-exchanger, Cardiopulmonary Bypass (product code DTR), Class II - Special Controls.

Submitted by Scimed (Minneapolis, US). The FDA issued a Cleared decision on December 6, 1990 after a review of 86 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.4240 - 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 Scimed devices

FDA 510(k) Submission Details - K904171

510(k) Number K904171 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 11, 1990
Decision Date December 06, 1990
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.

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 85
Devices cleared under the same product code (DTR) and FDA review panel - the closest regulatory comparables to K904171.
MYOCARD PROTECT SYST W/BLOOD CARDIO HEAT EXC/MODIF
K914742 · Medtronic Vascular · Dec 1991
MYOCARDIAL PROTECTION SYSTEM
K905500 · Medtronic Vascular · Jun 1991
BCD ADVANCED
K910923 · Shiley, Inc. · Apr 1991
SPBC SERIES SINGLE PASS BLOOD CARDIOPLEGIA SYSTEM
K896807 · Gish Biomedical, Inc. · Jul 1990
EXTRACORPOREAL HEAT EXCHANGER HE SERIES
K896020 · Gish Biomedical, Inc. · May 1990
MODIFIED MP-4 CARDIOPLEGIA DELIVERY SYSTEM W/CONDU
K900640 · 3M Company · Apr 1990