Cleared Traditional

K851496 - ECG MONITOR MODEL RM102

K851496 is an FDA 510(k) clearance for ECG MONITOR MODEL RM102, manufactured by Honeywell, Inc.. The device is a Class 2 Cardiovascular device with product code DXJ cleared through the Traditional 510(k) pathway after a 100-day FDA review.

K851496 · Honeywell, Inc. · Cardiovascular device
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Jul 1985
Decision
100d
Days
Class 2
Risk

K851496 is an FDA 510(k) clearance for the ECG MONITOR MODEL RM102. Classified as Display, Cathode-ray Tube, Medical (product code DXJ), Class II - Special Controls.

Submitted by Honeywell, Inc. (Pleasantville, US). The FDA issued a Cleared decision on July 24, 1985 after a review of 100 days - within the typical 510(k) review window.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2450 - 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 Honeywell, Inc. devices

FDA 510(k) Submission Details - K851496

510(k) Number K851496 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 15, 1985
Decision Date July 24, 1985
Days to Decision 100 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
25d faster than avg
Panel avg: 125d · This submission: 100d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DXJ Device Classification - Class 2, Special Controls

Product Code DXJ Display, Cathode-ray Tube, Medical
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2450
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 - DXJ Display, Cathode-ray Tube, Medical

All 57
Devices cleared under the same product code (DXJ) and FDA review panel - the closest regulatory comparables to K851496.
Q-CATH RM
K883031 · Quinton, Inc. · Sep 1988
M300 MONITOR/CONTROLLER T500 TREADMILL
K873774 · Burdick Corp. · Nov 1987
VM 781 SLAVE SCOPE
K854372 · Nihon Kohden America, Inc. · Feb 1986
SIRECUST 420 PATIENT DIALOG MONITOR
K851400 · Siemens Medical Solutions USA, Inc. · Jun 1985
DISPLAY MONITOR (VD-711RA-VD-712RA)
K850343 · Nihon Kohden America, Inc. · Apr 1985
SERVOMED MEDIVISION SCOPE SMV-235
K840209 · Litton Medical Electronics · Sep 1984