Cleared Abbreviated

K083287 - AVIVO MOBILE PATIENT MANAGEMENT SYSTEM

K083287 is an FDA 510(k) clearance for AVIVO MOBILE PATIENT MANAGEMENT SYSTEM, manufactured by Corventis, Inc.. The device is a Class 2 Cardiovascular device with product code DSI cleared through the Abbreviated 510(k) pathway after a 88-day FDA review.

K083287 · Corventis, Inc. · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 2009
Decision
88d
Days
Class 2
Risk

K083287 is an FDA 510(k) clearance for the AVIVO MOBILE PATIENT MANAGEMENT SYSTEM. Classified as Detector And Alarm, Arrhythmia (product code DSI), Class II - Special Controls.

Submitted by Corventis, Inc. (San Jose, US). The FDA issued a Cleared decision on February 3, 2009 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 Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Corventis, Inc. devices

FDA 510(k) Submission Details - K083287

510(k) Number K083287 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 07, 2008
Decision Date February 03, 2009
Days to Decision 88 days
Submission Type Abbreviated
Review Panel Cardiovascular (CV)
Summary Summary PDF
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
Standards-based clearance path.

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 263
Devices cleared under the same product code (DSI) and FDA review panel - the closest regulatory comparables to K083287.
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K082633 · Philips Medizinsysteme Boeblingen GmbH, Cardiac AN · Oct 2008