Cleared Traditional

K933014 - LIFESTREAM CENTRIFUGEL PUMP INTERFACE #...

K933014 is an FDA 510(k) clearance for LIFESTREAM CENTRIFUGEL PUMP INTERFACE #..., manufactured by St. Jude Medical, Inc.. The device is a Class 2 Cardiovascular device with product code KFM cleared through the Traditional 510(k) pathway after a 464-day FDA review.

K933014 · St. Jude Medical, Inc. · Cardiovascular device
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Sep 1994
Decision
464d
Days
Class 2
Risk

K933014 is an FDA 510(k) clearance for the LIFESTREAM CENTRIFUGEL PUMP INTERFACE #210PI. Classified as Pump, Blood, Cardiopulmonary Bypass, Non-roller Type (product code KFM), Class II - Special Controls.

Submitted by St. Jude Medical, Inc. (Chelmsford, US). The FDA issued a Cleared decision on September 28, 1994 after a review of 464 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.4360 - 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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Cardiovascular submissions.

View all St. Jude Medical, Inc. devices

FDA 510(k) Submission Details - K933014

510(k) Number K933014 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 21, 1993
Decision Date September 28, 1994
Days to Decision 464 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
339d slower than avg
Panel avg: 125d · This submission: 464d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KFM Device Classification - Class 2, Special Controls

Product Code KFM Pump, Blood, Cardiopulmonary Bypass, Non-roller Type
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.4360
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 - KFM Pump, Blood, Cardiopulmonary Bypass, Non-roller Type

All 55
Devices cleared under the same product code (KFM) and FDA review panel - the closest regulatory comparables to K933014.
CAPIOX SP PUMP HEAD
K962981 · Terumo Medical Corp. · Feb 1997
SARNS CENTRIFUGAL PUMP WITH DURAFLO II TREATMENT
K952879 · Baxter Healthcare Corp · Apr 1996
CAPIOX SP PUMP HEAD
K943861 · Terumo Corp. · Aug 1995
SARNS 8000 DELPHIN II CENTRI PUMP MOD W/INTEGR BAT
K915547 · 3M Health Care, Sarns · Sep 1993
SARNS 7850 CENTRIFUGAL PUMP (MODIFIED)
K915363 · 3M Health Care, Ltd. · Jul 1993
LIFESTREAM CENTRIFUGAL PUMP SYSTEM MODEL 2100CP
K921550 · St. Jude Medical, Inc. · May 1992