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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
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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
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
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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