Cleared Traditional

K843229 - LIFEPAK 200

K843229 is an FDA 510(k) clearance for LIFEPAK 200, manufactured by Physio-Control Corp.. The device is a Class 2 Cardiovascular device with product code LDD cleared through the Traditional 510(k) pathway after a 62-day FDA review.

K843229 · Physio-Control Corp. · Cardiovascular device
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Oct 1984
Decision
62d
Days
Class 2
Risk

K843229 is an FDA 510(k) clearance for the LIFEPAK 200. Classified as Dc-defibrillator, Low-energy, (including Paddles) (product code LDD), Class II - Special Controls.

Submitted by Physio-Control Corp. (Redmond, US). The FDA issued a Cleared decision on October 18, 1984 after a review of 62 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.5300 - 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 Physio-Control Corp. devices

FDA 510(k) Submission Details - K843229

510(k) Number K843229 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 17, 1984
Decision Date October 18, 1984
Days to Decision 62 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
63d faster than avg
Panel avg: 125d · This submission: 62d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LDD Device Classification - Class 2, Special Controls

Product Code LDD Dc-defibrillator, Low-energy, (including Paddles)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.5300
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 - LDD Dc-defibrillator, Low-energy, (including Paddles)

All 100
Devices cleared under the same product code (LDD) and FDA review panel - the closest regulatory comparables to K843229.
M/D4 W/CHARGER (CARDIOPAC 3M11)
K844447 · Datascope Corp. · Jan 1985
LS-260G MONITOR/RECORDER & DEFIBILLATOR
K843396 · Life Science Instrumentation, Inc. · Oct 1984
LIFEPAK 8
K842624 · Physio-Control Corp. · Oct 1984
EXTERNAL PEDIATRIC DEFIBRILLATOR PADDLE
K842667 · Marquette Electronics, Inc. · Aug 1984
TEC-3500 DEFIBRILLATOR
K840258 · Nihon Kohden America, Inc. · May 1984
MINI-DEFIBRILLATOR 280/4
K840246 · Life Science Instrumentation, Inc. · Apr 1984