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FDA 510(k)

AVIVO MOBILE PATIENT MANAGEMENT

K-Number: K113187 · 2012-01-04

ApplicantCorventis, Inc.
Decision Date2012-01-04
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AVIVO MOBILE PATIENT MANAGEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Corventis, Inc.. It received FDA 510(k) clearance on 2012-01-04 under 510(k) number K113187. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AVIVO MOBILE PATIENT MANAGEMENT?

AVIVO MOBILE PATIENT MANAGEMENT is a medical device that received FDA 510(k) clearance on 2012-01-04. The listed applicant is Corventis, Inc.. The 510(k) number is K113187.

When did AVIVO MOBILE PATIENT MANAGEMENT receive FDA 510(k) clearance?

AVIVO MOBILE PATIENT MANAGEMENT received FDA 510(k) clearance on 2012-01-04, under 510(k) number K113187.

Who is the listed applicant for AVIVO MOBILE PATIENT MANAGEMENT?

The FDA 510(k) record lists Corventis, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AVIVO MOBILE PATIENT MANAGEMENT?

The FDA product code for AVIVO MOBILE PATIENT MANAGEMENT is MHX.

Related Clinical Trials

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Other records listing Corventis, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K113372NUVANT, MOBILC CARDIAC TELEMETRYK111917NUVANT, MOBILE CARDIAC TELEMETRYK091971AVIVO MOBILE PATIENT MANAGEMENT SYSTEM, NUVANT MOBILE CARDIAC TELEMETRY (MCT) SYSTEMK090696NUVANT CARDIAC EVENT MONITORING SYSTEM; NUVANT MOBILE CARDIAC TELEMETRY SYSTEMK083287AVIVO MOBILE PATIENT MANAGEMENT SYSTEM

Related Devices (Code: MHX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260656Carescape ONE; Carescape Dock F0; TruSignal ECG MM; TruSignal PRES MM; TruSignal TEMP MM; TruSignal SpO2 MM 1.8M; TruSignal SpO2 MM 3.0MGE Healthcare Finland OyK260343Carescape Canvas 1000; Carescape Canvas Smart DisplayGE Healthcare Finland OyK260579Infinity® Acute Care System (IACS) – VG8.1Draeger Medical Systems, Inc.K251508Telemetry Monitor (iT30, iT50)Edan Instruments, Inc.K253277Monitor B105M; Monitor B125M; Monitor B155M; Monitor B105P; Monitor B125PGe Medical Systems Information Technologies, Inc.K254209Radius VSM and AccessoriesMasimo Corporation

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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