Cleared Traditional

K881905 - MODEL MICRO SI AMBULATORY ECG MONITOR

K881905 is an FDA 510(k) clearance for MODEL MICRO SI AMBULATORY ECG MONITOR, manufactured by Advanced Medical Products, Inc.. The device is a Class 2 Cardiovascular device with product code DSI cleared through the Traditional 510(k) pathway after a 88-day FDA review.

K881905 · Advanced Medical Products, Inc. · Cardiovascular device
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Aug 1988
Decision
88d
Days
Class 2
Risk

K881905 is an FDA 510(k) clearance for the MODEL MICRO SI AMBULATORY ECG MONITOR. Classified as Detector And Alarm, Arrhythmia (product code DSI), Class II - Special Controls.

Submitted by Advanced Medical Products, Inc. (Liverpool, US). The FDA issued a Cleared decision on August 2, 1988 after a review of 88 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 Advanced Medical Products, Inc. devices

FDA 510(k) Submission Details - K881905

510(k) Number K881905 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 06, 1988
Decision Date August 02, 1988
Days to Decision 88 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
37d faster than avg
Panel avg: 125d · This submission: 88d
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 235
Devices cleared under the same product code (DSI) and FDA review panel - the closest regulatory comparables to K881905.
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