Cleared Traditional

K910494 - RESTING EKG ELECTRODE SERIES

K910494 is an FDA 510(k) clearance for RESTING EKG ELECTRODE SERIES, manufactured by Medtronic Andover Medical, Inc.. The device is a Class 2 Cardiovascular device with product code DRX cleared through the Traditional 510(k) pathway after a 76-day FDA review.

K910494 · Medtronic Andover Medical, Inc. · Cardiovascular device
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Apr 1991
Decision
76d
Days
Class 2
Risk

K910494 is an FDA 510(k) clearance for the RESTING EKG ELECTRODE SERIES. Classified as Electrode, Electrocardiograph (product code DRX), Class II - Special Controls.

Submitted by Medtronic Andover Medical, Inc. (Haverhill, US). The FDA issued a Cleared decision on April 22, 1991 after a review of 76 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2360 - 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 Medtronic Andover Medical, Inc. devices

FDA 510(k) Submission Details - K910494

510(k) Number K910494 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 05, 1991
Decision Date April 22, 1991
Days to Decision 76 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
49d faster than avg
Panel avg: 125d · This submission: 76d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DRX Device Classification - Class 2, Special Controls

Product Code DRX Electrode, Electrocardiograph
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2360
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 - DRX Electrode, Electrocardiograph

All 183
Devices cleared under the same product code (DRX) and FDA review panel - the closest regulatory comparables to K910494.
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MODEL 1850 ELECTRODE
K903918 · Medtronic Vascular · Oct 1990