Cleared Traditional

K873682 - FERRIS ECG ELECTRODE W/HYDROGEL

K873682 is an FDA 510(k) clearance for FERRIS ECG ELECTRODE W/HYDROGEL, manufactured by Ferris Mfg. Corp.. The device is a Class 2 Cardiovascular device with product code DRX cleared through the Traditional 510(k) pathway after a 106-day FDA review.

K873682 · Ferris Mfg. Corp. · Cardiovascular device
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Dec 1987
Decision
106d
Days
Class 2
Risk

K873682 is an FDA 510(k) clearance for the FERRIS ECG ELECTRODE W/HYDROGEL. Classified as Electrode, Electrocardiograph (product code DRX), Class II - Special Controls.

Submitted by Ferris Mfg. Corp. (Burr Ridge, US). The FDA issued a Cleared decision on December 29, 1987 after a review of 106 days - within the typical 510(k) review window.

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: Standard predicate-based submission. Standard predicate reliance. 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 Ferris Mfg. Corp. devices

FDA 510(k) Submission Details - K873682

510(k) Number K873682 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 14, 1987
Decision Date December 29, 1987
Days to Decision 106 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
19d faster than avg
Panel avg: 125d · This submission: 106d
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 K873682.
TRACETS 3000
K875015 · Lectec Corp. · Jan 1988
FOAM BORDERED DIAGNOSTIC (CARE) ELECTRODE
K875041 · Labeltape Meditect, Inc. · Jan 1988
TRAUMA-TRODE, ECG ELECTRODE (597 ADHESIVE)
K874437 · Labeltape Meditect, Inc. · Dec 1987
RESUBMITTED STANDARD MICROPORE ECG ELECTRODE
K874628 · Labeltape Meditect, Inc. · Dec 1987
NEONATAL SPUNLACE BREATHABLE POLY. FABRIC ECG(RCR)
K872871 · Labeltape Meditect, Inc. · Oct 1987
MACTRODE-II
K872784 · Marquette Electronics, Inc. · Oct 1987