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FDA 510(k)

NUVON VITALS CHARTING SYSTEM

K-Number: K130234 · 2013-03-13

ApplicantNuvon, Inc.
Decision Date2013-03-13
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NUVON VITALS CHARTING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Nuvon, Inc.. It received FDA 510(k) clearance on 2013-03-13 under 510(k) number K130234. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NUVON VITALS CHARTING SYSTEM?

NUVON VITALS CHARTING SYSTEM is a medical device that received FDA 510(k) clearance on 2013-03-13. The listed applicant is Nuvon, Inc.. The 510(k) number is K130234.

When did NUVON VITALS CHARTING SYSTEM receive FDA 510(k) clearance?

NUVON VITALS CHARTING SYSTEM received FDA 510(k) clearance on 2013-03-13, under 510(k) number K130234.

Who is the listed applicant for NUVON VITALS CHARTING SYSTEM?

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

What is the FDA product code for NUVON VITALS CHARTING SYSTEM?

The FDA product code for NUVON VITALS CHARTING SYSTEM is MWI.

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 Nuvon, 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.

K102135VECTOR EVENT GRID ARCHITECTURE (VEGA) SYSTEM

Related Devices (Code: MWI)

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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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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