FDA 510(k), K091971, AVIVO MOBILE PATIENT MANAGEMENT SYSTEM, NUVANT MOBILE CARDIAC TELEMETRY (MCT) SYSTEM

FDA 510(k), K091971, AVIVO MOBILE PATIENT MANAGEMENT SYSTEM, NUVANT MOBILE CARDIAC TELEMETRY (MCT) SYSTEM

Regular price $49.00 USD
Regular price Sale price $49.00 USD
Sale Sold out
510(K) Number: K091971
Device Name: AVIVO MOBILE PATIENT MANAGEMENT SYSTEM, NUVANT MOBILE CARDIAC TELEMETRY (MCT) SYSTEM
Manufacturer: CORVENTIS, INC.
Device Classification Name: detector and alarm, arrhythmia
Regulation Number: 870.1025
Classification Product Code: DSI
Date Received: 07/01/2009
Decision Date: 08/27/2009
Regulation Medical Specialty: Cardiovascular

NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.

View full details