Cleared Traditional

K934254 - IMPULSE 3000 DEFIBRILLATOR ANALYZER

K934254 is an FDA 510(k) clearance for IMPULSE 3000 DEFIBRILLATOR ANALYZER, manufactured by Dynatech/Nevada, Inc.. The device is a Class 2 Cardiovascular device with product code DRL cleared through the Traditional 510(k) pathway after a 84-day FDA review.

K934254 · Dynatech/Nevada, Inc. · Cardiovascular device
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Nov 1993
Decision
84d
Days
Class 2
Risk

K934254 is an FDA 510(k) clearance for the IMPULSE 3000 DEFIBRILLATOR ANALYZER. Classified as Tester, Defibrillator (product code DRL), Class II - Special Controls.

Submitted by Dynatech/Nevada, Inc. (Washington, US). The FDA issued a Cleared decision on November 23, 1993 after a review of 84 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.5325 - 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 Dynatech/Nevada, Inc. devices

FDA 510(k) Submission Details - K934254

510(k) Number K934254 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 31, 1993
Decision Date November 23, 1993
Days to Decision 84 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
41d faster than avg
Panel avg: 125d · This submission: 84d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DRL Device Classification - Class 2, Special Controls

Product Code DRL Tester, Defibrillator
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.5325
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 - DRL Tester, Defibrillator

All 14
Devices cleared under the same product code (DRL) and FDA review panel - the closest regulatory comparables to K934254.
DEFIBRILLATOR ANALYZER, DELTA 1000
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K904159 · Bio-Tek Instruments, Inc. · Mar 1991
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K790394 · Physio-Control Corp. · Mar 1979
CARDIAC CARE Q/C TEST KIT
K782033 · Instrumentation Laboratory CO · Dec 1978