Cleared Traditional

K982264 - FIRSTSAVE BIPHASIC MODELS 9200 AND 9210

K982264 is an FDA 510(k) clearance for FIRSTSAVE BIPHASIC MODELS 9200 AND 9210, manufactured by Survivalink Corp.. The device is a Class 3 Cardiovascular device with product code MKJ cleared through the Traditional 510(k) pathway after a 210-day FDA review.

K982264 · Survivalink Corp. · Cardiovascular device
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Jan 1999
Decision
210d
Days
Class 3
Risk

K982264 is an FDA 510(k) clearance for the FIRSTSAVE BIPHASIC MODELS 9200 AND 9210. Classified as Automated External Defibrillators (non-wearable) (product code MKJ), Class III - Premarket Approval.

Submitted by Survivalink Corp. (Minnetonka, US). The FDA issued a Cleared decision on January 25, 1999 after a review of 210 days - an extended review 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 Survivalink Corp. devices

FDA 510(k) Submission Details - K982264

510(k) Number K982264 FDA.gov
FDA Decision Cleared Substantially Equivalent - Third Party Review (ST)
Date Received June 29, 1998
Decision Date January 25, 1999
Days to Decision 210 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
85d slower than avg
Panel avg: 125d · This submission: 210d
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 143
Devices cleared under the same product code (MKJ) and FDA review panel - the closest regulatory comparables to K982264.
ZOLL SUPERPADZ ADULT MULTI-FUNCTION ELECTRODES, MODEL 8900-XXXX
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ZOLL FIRST RESPONDER PADZ ADULT DEFIBRILLATION ELECTRODES
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K984286 · Hewlett-Packard Co. · Dec 1998
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K981737 · Katecho, Inc. · Dec 1998
ZOLL STAT*PADZ ADULT MULTI-FUNCTION ELECTRODES MODEL NUMBER 8900-4003
K981802 · Bio-Detek, Inc. · Nov 1998