Cleared Traditional

K892065 - LIFEPAK 250 DEFIBRILLATOR/MONITOR

K892065 is an FDA 510(k) clearance for LIFEPAK 250 DEFIBRILLATOR/MONITOR, manufactured by Physio-Control Corp.. The device is a Class 3 Cardiovascular device with product code MKJ cleared through the Traditional 510(k) pathway after a 67-day FDA review.

K892065 · Physio-Control Corp. · Cardiovascular device
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Jun 1989
Decision
67d
Days
Class 3
Risk

K892065 is an FDA 510(k) clearance for the LIFEPAK 250 DEFIBRILLATOR/MONITOR. Classified as Automated External Defibrillators (non-wearable) (product code MKJ), Class III - Premarket Approval.

Submitted by Physio-Control Corp. (Redmond, US). The FDA issued a Cleared decision on June 5, 1989 after a review of 67 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.5310 - 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. High regulatory complexity profile. This clearance follows a standard predicate-based equivalence path within the Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

View all Physio-Control Corp. devices

FDA 510(k) Submission Details - K892065

510(k) Number K892065 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 30, 1989
Decision Date June 05, 1989
Days to Decision 67 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
58d faster than avg
Panel avg: 125d · This submission: 67d
Pathway characteristics
Predicate-based equivalence.

MKJ Device Classification - Class 3, Premarket Approval

Product Code MKJ Automated External Defibrillators (non-wearable)
Device Class Class 3 - Premarket Approval
CFR Regulation 21 CFR 870.5310
Definition This Device Is A Non-wearable Prescription Use Only Aed. These Are Devices That Include Automated External Defibrillation. Automated External Defibrillators Use External Pad-type Electrodes To Sense, Detect, Classify And Treat (with An Electrical Shock) Ventricular Fibrillation. These Devices Are Intended To Be Used On Suspected Victims Of Sudden Cardiac Arrest. A Person In Cardiac Arrest Is Unresponsive And Is Not Breathing Normally. The Device Can Be Sold With Prescription Only.
What this classification means

Class III devices typically require Premarket Approval (PMA) with clinical evidence. Clearance through 510(k) for Class III devices is granted only when substantial equivalence to a valid predicate can be established.

Regulatory Peers - MKJ Automated External Defibrillators (non-wearable)

All 118
Devices cleared under the same product code (MKJ) and FDA review panel - the closest regulatory comparables to K892065.
D1400 DEFIBRILLATOR W/ DEFIBRILLATION ADVISORY OPT
K932931 · Zoll Medical Corp · Oct 1993
SERIES 1500 DEFIBRILLATOR, MODIFICATION
K926172 · Marquette Electronics, Inc. · Feb 1993
SHOCK ADVISORY ADAPTER FOR USE W/LIFEPAK 9
K892005 · Physio-Control Corp. · Jun 1989
MARQUETTE 1200 DEFIBRILLATOR
K882067 · Marquette Electronics, Inc. · Nov 1988
LIFEPAK 200
K853564 · Physio-Control Corp. · Oct 1985