Cleared Traditional

K862375 - CARDIO PORT 500 24-H ECG AMBULATORY MONITOR SYSTEM

K862375 is an FDA 510(k) clearance for CARDIO PORT 500 24-H ECG AMBULATORY MON..., manufactured by Grandcor Medical Systems. The device is a Class 2 Cardiovascular device with product code DSI cleared through the Traditional 510(k) pathway after a 7-day FDA review.

K862375 · Grandcor Medical Systems · Cardiovascular device
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Jul 1986
Decision
7d
Days
Class 2
Risk

K862375 is an FDA 510(k) clearance for the CARDIO PORT 500 24-H ECG AMBULATORY MONITOR SYSTEM. Classified as Detector And Alarm, Arrhythmia (product code DSI), Class II - Special Controls.

Submitted by Grandcor Medical Systems (Dayton, US). The FDA issued a Cleared decision on July 1, 1986 after a review of 7 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1025 - 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 Grandcor Medical Systems devices

FDA 510(k) Submission Details - K862375

510(k) Number K862375 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 24, 1986
Decision Date July 01, 1986
Days to Decision 7 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
118d faster than avg
Panel avg: 125d · This submission: 7d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DSI Device Classification - Class 2, Special Controls

Product Code DSI Detector And Alarm, Arrhythmia
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1025
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 - DSI Detector And Alarm, Arrhythmia

All 303
Devices cleared under the same product code (DSI) and FDA review panel - the closest regulatory comparables to K862375.
CASE 12
K862316 · Marquette Electronics, Inc. · Nov 1986
MODEL 6000 AMBULATORY ECG ANALYSIS SYSTEM
K863724 · Oxford Medilog, Inc. · Nov 1986
Q4000 AND Q3040 ELECTROCARDIOGRAPH MONITOR
K863159 · Quinton, Inc. · Oct 1986
PC ARRHYTHMIA DETECTION/ANALYSIS - ARRHYTHMIA III
K860980 · Spacelabs, Inc. · May 1986
595 ARRHYTHMIA MONITORING SYSTEM
K852250 · Burdick Corp. · May 1986
SCM-400 HOLTER SYSTEM
K860950 · Fukuda Denshi USA, Inc. · May 1986