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FDA 510(k)

NUVANT, MOBILE CARDIAC TELEMETRY

K-Number: K111917 · 2011-08-24

ApplicantCorventis, Inc.
Decision Date2011-08-24
Product CodeQYX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NUVANT, MOBILE CARDIAC TELEMETRY is the device name listed in this FDA 510(k) record. The listed applicant is Corventis, Inc.. It received FDA 510(k) clearance on 2011-08-24 under 510(k) number K111917. The device is classified under product code QYX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NUVANT, MOBILE CARDIAC TELEMETRY?

NUVANT, MOBILE CARDIAC TELEMETRY is a medical device that received FDA 510(k) clearance on 2011-08-24. The listed applicant is Corventis, Inc.. The 510(k) number is K111917.

When did NUVANT, MOBILE CARDIAC TELEMETRY receive FDA 510(k) clearance?

NUVANT, MOBILE CARDIAC TELEMETRY received FDA 510(k) clearance on 2011-08-24, under 510(k) number K111917.

Who is the listed applicant for NUVANT, MOBILE CARDIAC TELEMETRY?

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 NUVANT, MOBILE CARDIAC TELEMETRY?

The FDA product code for NUVANT, MOBILE CARDIAC TELEMETRY is QYX.

Related Clinical Trials

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.

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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 TELEMETRYK113187AVIVO MOBILE PATIENT MANAGEMENTK091971AVIVO 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: QYX)

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.

K250793RhythmStar System (SL)RhythMedix, LLCK241179Rhythm Express Remote Cardiac Monitoring System (RX-1 mini)VivaQuant, Inc.K240653SmartCardia 7L Platform (MCT)Smartcardia SAK240029Zio AT® device (A100A1001)iRhythm Technologies, Inc.K233584RhythmStar SystemRhythMedix, LLCK162956NOWCARDIO SYSTEMContex International Technologies (Canada), Inc.

Official Source

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

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